Canonical Allele Identifier: CA919844488
Gene: BRCA1 HGNC NCBI

Linked Data

dbSNP Id: rs1567788870

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43091378_43091379del , CM000679.2:g.43091378_43091379del GRCh38
NC_000017.10:g.41243395_41243396del , CM000679.1:g.41243395_41243396del GRCh37
NC_000017.9:g.38496921_38496922del NCBI36
NG_005905.2:g.126606_126607del , LRG_292:g.126606_126607del

Transcript Alleles

HGVS Amino-acid Change
ENST00000354071.8:n.4217_4218del
ENST00000461574.2:c.4096+57_4096+58del ENSP00000417241.2:n.4096+57_4096+58del
ENST00000470026.6:c.4096+57_4096+58del ENSP00000419274.2:n.4096+57_4096+58del
ENST00000473961.6:c.3970+57_3970+58del ENSP00000420201.2:n.3970+57_3970+58del
ENST00000476777.6:c.4093+57_4093+58del ENSP00000417554.2:n.4093+57_4093+58del
ENST00000477152.6:c.4018+57_4018+58del ENSP00000419988.2:n.4018+57_4018+58del
ENST00000478531.6:c.785-346_785-345del ENSP00000420412.2:n.785-346_785-345del
ENST00000489037.2:c.4018+57_4018+58del ENSP00000420781.2:n.4018+57_4018+58del
ENST00000493919.6:c.647-346_647-345del ENSP00000418819.2:n.647-346_647-345del
ENST00000494123.6:c.4096+57_4096+58del ENSP00000419103.2:n.4096+57_4096+58del
ENST00000497488.2:c.3208+57_3208+58del ENSP00000418986.2:n.3208+57_3208+58del
ENST00000618469.2:c.4096+57_4096+58del ENSP00000478114.2:n.4096+57_4096+58del
ENST00000634433.2:c.3973+57_3973+58del ENSP00000489431.2:n.3973+57_3973+58del
ENST00000644379.2:c.4096+57_4096+58del ENSP00000496570.2:n.4096+57_4096+58del
ENST00000644555.2:c.647-346_647-345del ENSP00000494614.2:n.647-346_647-345del
ENST00000652672.2:c.3955+57_3955+58del ENSP00000498906.2:n.3955+57_3955+58del
ENST00000484087.6:c.665-346_665-345del ENSP00000419481.2:n.665-346_665-345del
ENST00000700182.1:c.707-346_707-345del ENSP00000514849.1:n.707-346_707-345del
ENST00000357654.9:c.4096+57_4096+58del MANE Select ENSP00000350283.3:n.4096+57_4096+58del
ENST00000471181.7:c.4096+57_4096+58del ENSP00000418960.2:n.4096+57_4096+58del
ENST00000644379.1:c.417+57_417+58del
ENST00000352993.7:c.671-346_671-345del ENSP00000312236.5:n.671-346_671-345del
ENST00000354071.7:c.4153_4154del ENSP00000326002.7:p.Val1385LeufsTer14
ENST00000357654.7:c.4096+57_4096+58del ENSP00000350283.3:n.4096+57_4096+58del
ENST00000461221.5:c.*3879+57_*3879+58del ENSP00000418548.1:n.*3879+57_*3879+58del
ENST00000461574.1:c.390+57_390+58del
ENST00000468300.5:c.788-346_788-345del ENSP00000417148.1:n.788-346_788-345del
ENST00000471181.6:c.4096+57_4096+58del ENSP00000418960.2:n.4096+57_4096+58del
ENST00000478531.5:c.785-346_785-345del ENSP00000420412.1:n.785-346_785-345del
ENST00000484087.5:c.410-346_410-345del ENSP00000419481.1:n.410-346_410-345del
ENST00000487825.5:c.413-346_413-345del ENSP00000418212.1:n.413-346_413-345del
ENST00000491747.6:c.788-346_788-345del ENSP00000420705.2:n.788-346_788-345del
ENST00000493795.5:c.3955+57_3955+58del ENSP00000418775.1:n.3955+57_3955+58del
ENST00000493919.5:c.647-346_647-345del ENSP00000418819.1:n.647-346_647-345del
ENST00000586385.5:c.5-27427_5-27426del ENSP00000465818.1:n.5-27427_5-27426del
ENST00000591534.5:c.-43-16857_-43-16856del ENSP00000467329.1:n.-43-16857_-43-16856del
ENST00000591849.5:c.-99+33893_-99+33894del ENSP00000465347.1:n.-99+33893_-99+33894del
NM_007294.3:c.4096+57_4096+58del , LRG_292t1:c.4096+57_4096+58del NP_009225.1:n.4096+57_4096+58del
NM_007297.3:c.3955+57_3955+58del NP_009228.2:n.3955+57_3955+58del
NM_007298.3:c.788-346_788-345del NP_009229.2:n.788-346_788-345del
NM_007299.3:c.788-346_788-345del NP_009230.2:n.788-346_788-345del
NM_007300.3:c.4096+57_4096+58del NP_009231.2:n.4096+57_4096+58del
NR_027676.1:n.4232+57_4232+58del
NM_007294.4:c.4096+57_4096+58del MANE Select NP_009225.1:n.4096+57_4096+58del
NM_007297.4:c.3955+57_3955+58del NP_009228.2:n.3955+57_3955+58del
NM_007299.4:c.788-346_788-345del NP_009230.2:n.788-346_788-345del
NM_007300.4:c.4096+57_4096+58del NP_009231.2:n.4096+57_4096+58del
NR_027676.2:n.4273+57_4273+58del