Canonical Allele Identifier: CA10591270
Community Standard Title: NM_007294.4(BRCA1):c.5136G>C (p.Trp1712Cys)
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43063890C>G , CM000679.2:g.43063890C>G GRCh38
NC_000017.10:g.41215907C>G , CM000679.1:g.41215907C>G GRCh37
NC_000017.9:g.38469433C>G NCBI36
NG_005905.2:g.154094G>C , LRG_292:g.154094G>C

Transcript Alleles

HGVS Amino-acid Change
NM_007294.4:c.5136G>C MANE Select NP_009225.1:p.Trp1712Cys
ENST00000357654.9:c.5136G>C MANE Select ENSP00000350283.3:p.Trp1712Cys
NM_007294.3:c.5136G>C , LRG_292t1:c.5136G>C NP_009225.1:p.Trp1712Cys
NM_007297.3:c.4995G>C NP_009228.2:p.Trp1665Cys
NM_007297.4:c.4995G>C NP_009228.2:p.Trp1665Cys
NM_007298.3:c.1824G>C NP_009229.2:p.Trp608Cys
NM_007299.3:c.1824G>C NP_009230.2:p.Trp608Cys
NM_007299.4:c.1824G>C NP_009230.2:p.Trp608Cys
NM_007300.3:c.5199G>C NP_009231.2:p.Trp1733Cys
NM_007300.4:c.5199G>C NP_009231.2:p.Trp1733Cys
NR_027676.1:n.5272G>C
NR_027676.2:n.5313G>C
ENST00000352993.7:c.1710G>C ENSP00000312236.5:p.Trp570Cys
ENST00000357654.7:c.5136G>C ENSP00000350283.3:p.Trp1712Cys
ENST00000461221.5:c.*4919G>C ENSP00000418548.1:n.*4919G>C
ENST00000461574.2:c.5133G>C ENSP00000417241.2:p.Trp1711Cys
ENST00000468300.5:c.1824G>C ENSP00000417148.1:p.Trp608Cys
ENST00000470026.6:c.5136G>C ENSP00000419274.2:p.Trp1712Cys
ENST00000471181.6:c.5199G>C ENSP00000418960.2:p.Trp1733Cys
ENST00000471181.7:c.5199G>C ENSP00000418960.2:p.Trp1733Cys
ENST00000473961.6:c.5010G>C ENSP00000420201.2:p.Trp1670Cys
ENST00000476777.6:c.5130G>C ENSP00000417554.2:p.Trp1710Cys
ENST00000477152.6:c.5058G>C ENSP00000419988.2:p.Trp1686Cys
ENST00000478531.5:c.1824G>C ENSP00000420412.1:p.Trp608Cys
ENST00000478531.6:c.1824G>C ENSP00000420412.2:p.Trp608Cys
ENST00000484087.5:c.1449G>C ENSP00000419481.1:p.Trp483Cys
ENST00000484087.6:c.1698G>C ENSP00000419481.2:p.Trp566Cys
ENST00000489037.2:c.5058G>C ENSP00000420781.2:p.Trp1686Cys
ENST00000491747.6:c.1824G>C ENSP00000420705.2:p.Trp608Cys
ENST00000493795.5:c.4995G>C ENSP00000418775.1:p.Trp1665Cys
ENST00000493919.5:c.1686G>C ENSP00000418819.1:p.Trp562Cys
ENST00000493919.6:c.1686G>C ENSP00000418819.2:p.Trp562Cys
ENST00000494123.6:c.5136G>C ENSP00000419103.2:p.Trp1712Cys
ENST00000497488.2:c.4248G>C ENSP00000418986.2:p.Trp1416Cys
ENST00000586385.5:c.66G>C ENSP00000465818.1:p.Trp22Cys
ENST00000591534.5:c.609G>C ENSP00000467329.1:p.Trp203Cys
ENST00000591849.5:c.-98-13700G>C ENSP00000465347.1:n.-98-13700G>C
ENST00000618469.2:c.5136G>C ENSP00000478114.2:p.Trp1712Cys
ENST00000634433.2:c.5013G>C ENSP00000489431.2:p.Trp1671Cys
ENST00000644379.1:c.1523G>C
ENST00000644379.2:c.5202G>C ENSP00000496570.2:p.Trp1734Cys
ENST00000644555.2:c.1686G>C ENSP00000494614.2:p.Trp562Cys
ENST00000652672.2:c.4995G>C ENSP00000498906.2:p.Trp1665Cys