Canonical Allele Identifier: CA002080
Gene: BRCA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 125613
ClinVar RCV Id: RCV000112022
dbSNP Id: rs80357883

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43092336_43092337insC , CM000679.2:g.43092336_43092337insC GRCh38
NC_000017.10:g.41244353_41244354insC , CM000679.1:g.41244353_41244354insC GRCh37
NC_000017.9:g.38497879_38497880insC NCBI36
NG_005905.2:g.125647_125648insG , LRG_292:g.125647_125648insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000354071.8:n.3258_3259insG
ENST00000461574.2:c.3194_3195insG ENSP00000417241.2:p.Asp1065GlufsTer2
ENST00000470026.6:c.3194_3195insG ENSP00000419274.2:p.Asp1065GlufsTer2
ENST00000473961.6:c.3068_3069insG ENSP00000420201.2:p.Asp1023GlufsTer2
ENST00000476777.6:c.3191_3192insG ENSP00000417554.2:p.Asp1064GlufsTer2
ENST00000477152.6:c.3116_3117insG ENSP00000419988.2:p.Asp1039GlufsTer2
ENST00000478531.6:c.785-1305_785-1304insG ENSP00000420412.2:n.785-1305_785-1304insG
ENST00000489037.2:c.3116_3117insG ENSP00000420781.2:p.Asp1039GlufsTer2
ENST00000493919.6:c.647-1305_647-1304insG ENSP00000418819.2:n.647-1305_647-1304insG
ENST00000494123.6:c.3194_3195insG ENSP00000419103.2:p.Asp1065GlufsTer2
ENST00000497488.2:c.2306_2307insG ENSP00000418986.2:p.Asp769GlufsTer2
ENST00000618469.2:c.3194_3195insG ENSP00000478114.2:p.Asp1065GlufsTer2
ENST00000634433.2:c.3071_3072insG ENSP00000489431.2:p.Asp1024GlufsTer2
ENST00000644379.2:c.3194_3195insG ENSP00000496570.2:p.Asp1065GlufsTer2
ENST00000644555.2:c.647-1305_647-1304insG ENSP00000494614.2:n.647-1305_647-1304insG
ENST00000652672.2:c.3053_3054insG ENSP00000498906.2:p.Asp1018GlufsTer2
ENST00000484087.6:c.665-1305_665-1304insG ENSP00000419481.2:n.665-1305_665-1304insG
ENST00000700182.1:c.707-1305_707-1304insG ENSP00000514849.1:n.707-1305_707-1304insG
ENST00000357654.9:c.3194_3195insG MANE Select ENSP00000350283.3:p.Asp1065GlufsTer2
ENST00000471181.7:c.3194_3195insG ENSP00000418960.2:p.Asp1065GlufsTer2
ENST00000352993.7:c.671-1305_671-1304insG ENSP00000312236.5:n.671-1305_671-1304insG
ENST00000354071.7:c.3194_3195insG ENSP00000326002.7:p.Asp1065GlufsTer2
ENST00000357654.7:c.3194_3195insG ENSP00000350283.3:p.Asp1065GlufsTer2
ENST00000461221.5:c.*2977_*2978insG ENSP00000418548.1:n.*2977_*2978insG
ENST00000468300.5:c.788-1305_788-1304insG ENSP00000417148.1:n.788-1305_788-1304insG
ENST00000471181.6:c.3194_3195insG ENSP00000418960.2:p.Asp1065GlufsTer2
ENST00000478531.5:c.785-1305_785-1304insG ENSP00000420412.1:n.785-1305_785-1304insG
ENST00000484087.5:c.410-1305_410-1304insG ENSP00000419481.1:n.410-1305_410-1304insG
ENST00000487825.5:c.413-1305_413-1304insG ENSP00000418212.1:n.413-1305_413-1304insG
ENST00000491747.6:c.788-1305_788-1304insG ENSP00000420705.2:n.788-1305_788-1304insG
ENST00000493795.5:c.3053_3054insG ENSP00000418775.1:p.Asp1018GlufsTer2
ENST00000493919.5:c.647-1305_647-1304insG ENSP00000418819.1:n.647-1305_647-1304insG
ENST00000586385.5:c.5-28386_5-28385insG ENSP00000465818.1:n.5-28386_5-28385insG
ENST00000591534.5:c.-43-17816_-43-17815insG ENSP00000467329.1:n.-43-17816_-43-17815insG
ENST00000591849.5:c.-99+32934_-99+32935insG ENSP00000465347.1:n.-99+32934_-99+32935insG
NM_007294.3:c.3194_3195insG , LRG_292t1:c.3194_3195insG NP_009225.1:p.Asp1065GlufsTer2
NM_007297.3:c.3053_3054insG NP_009228.2:p.Asp1018GlufsTer2
NM_007298.3:c.788-1305_788-1304insG NP_009229.2:n.788-1305_788-1304insG
NM_007299.3:c.788-1305_788-1304insG NP_009230.2:n.788-1305_788-1304insG
NM_007300.3:c.3194_3195insG NP_009231.2:p.Asp1065GlufsTer2
NR_027676.1:n.3330_3331insG
NM_007294.4:c.3194_3195insG MANE Select NP_009225.1:p.Asp1065GlufsTer2
NM_007297.4:c.3053_3054insG NP_009228.2:p.Asp1018GlufsTer2
NM_007299.4:c.788-1305_788-1304insG NP_009230.2:n.788-1305_788-1304insG
NM_007300.4:c.3194_3195insG NP_009231.2:p.Asp1065GlufsTer2
NR_027676.2:n.3371_3372insG