Canonical Allele Identifier: CA341337986
Gene: AGL HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.100376375A>T (hg19) chr1:g.99910819A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.99910819A>T , CM000663.2:g.99910819A>T GRCh38
NC_000001.10:g.100376375A>T , CM000663.1:g.100376375A>T GRCh37
NC_000001.9:g.100148963A>T NCBI36
NG_012865.1:g.65736A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000361915.8:c.3808A>T MANE Select ENSP00000355106.3:p.Arg1270Ter
ENST00000637337.1:n.4019A>T
ENST00000294724.8:c.3808A>T ENSP00000294724.4:p.Arg1270Ter
ENST00000361302.7:c.3760A>T ENSP00000354971.3:p.Arg1254Ter
ENST00000361522.4:c.3757A>T ENSP00000354635.4:p.Arg1253Ter
ENST00000361915.7:c.3808A>T ENSP00000355106.3:p.Arg1270Ter
ENST00000370161.6:c.3760A>T ENSP00000359180.2:p.Arg1254Ter
ENST00000370163.7:c.3808A>T ENSP00000359182.3:p.Arg1270Ter
ENST00000370165.7:c.3808A>T ENSP00000359184.3:p.Arg1270Ter
NM_000028.2:c.3808A>T NP_000019.2:p.Arg1270Ter
NM_000642.2:c.3808A>T NP_000633.2:p.Arg1270Ter
NM_000643.2:c.3808A>T NP_000634.2:p.Arg1270Ter
NM_000644.2:c.3808A>T NP_000635.2:p.Arg1270Ter
NM_000645.2:c.3757A>T NP_000636.2:p.Arg1253Ter
NM_000646.2:c.3760A>T NP_000637.2:p.Arg1254Ter
XM_005270557.1:c.3808A>T XP_005270614.1:p.Arg1270Ter
XM_005270557.2:c.3808A>T XP_005270614.1:p.Arg1270Ter
XM_017000501.2:c.2068A>T XP_016855990.1:p.Arg690Ter
NM_000642.3:c.3808A>T MANE Select NP_000633.2:p.Arg1270Ter
Search 100 bp 5'
Search 100 bp 3'