Canonical Allele Identifier: CA002890
Gene: BRCA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 55220
dbSNP Id: rs273900736

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43074490del , CM000679.2:g.43074490del GRCh38
NC_000017.10:g.41226507del , CM000679.1:g.41226507del GRCh37
NC_000017.9:g.38480033del NCBI36
NG_005905.2:g.143494del , LRG_292:g.143494del

Transcript Alleles

HGVS Amino-acid change
ENST00000461574.2:c.4513del ENSP00000417241.2:p.Asp1505IlefsTer?
ENST00000470026.6:c.4516del ENSP00000419274.2:p.Asp1506IlefsTer?
ENST00000473961.6:c.4390del ENSP00000420201.2:p.Asp1464IlefsTer?
ENST00000476777.6:c.4510del ENSP00000417554.2:p.Asp1504IlefsTer?
ENST00000477152.6:c.4438del ENSP00000419988.2:p.Asp1480IlefsTer?
ENST00000478531.6:c.1204del ENSP00000420412.2:p.Asp402IlefsTer?
ENST00000489037.2:c.4438del ENSP00000420781.2:p.Asp1480IlefsTer?
ENST00000493919.6:c.1066del ENSP00000418819.2:p.Asp356IlefsTer?
ENST00000494123.6:c.4516del ENSP00000419103.2:p.Asp1506IlefsTer?
ENST00000497488.2:c.3628del ENSP00000418986.2:p.Asp1210IlefsTer?
ENST00000618469.2:c.4516del ENSP00000478114.2:p.Asp1506IlefsTer?
ENST00000634433.2:c.4393del ENSP00000489431.2:p.Asp1465IlefsTer?
ENST00000644379.2:c.4582del ENSP00000496570.2:p.Asp1528IlefsTer?
ENST00000644555.2:c.1066del ENSP00000494614.2:p.Asp356IlefsTer?
ENST00000652672.2:c.4375del ENSP00000498906.2:p.Asp1459IlefsTer?
ENST00000484087.6:c.1078del ENSP00000419481.2:p.Asp360IlefsTer?
ENST00000700182.1:c.1123del ENSP00000514849.1:p.Asp375IlefsTer?
ENST00000357654.9:c.4516del MANE Select ENSP00000350283.3:p.Asp1506IlefsTer?
ENST00000471181.7:c.4579del ENSP00000418960.2:p.Asp1527IlefsTer?
ENST00000644379.1:c.903del
ENST00000352993.7:c.1090del ENSP00000312236.5:p.Asp364IlefsTer?
ENST00000357654.7:c.4516del ENSP00000350283.3:p.Asp1506IlefsTer?
ENST00000461221.5:c.*4299del ENSP00000418548.1:n.*4299del
ENST00000468300.5:c.1204del ENSP00000417148.1:p.Asp402IlefsTer?
ENST00000471181.6:c.4579del ENSP00000418960.2:p.Asp1527IlefsTer?
ENST00000478531.5:c.1204del ENSP00000420412.1:p.Asp402IlefsTer?
ENST00000484087.5:c.829del ENSP00000419481.1:p.Asp277IlefsTer?
ENST00000491747.6:c.1204del ENSP00000420705.2:p.Asp402IlefsTer?
ENST00000493795.5:c.4375del ENSP00000418775.1:p.Asp1459IlefsTer?
ENST00000493919.5:c.1066del ENSP00000418819.1:p.Asp356IlefsTer?
ENST00000586385.5:c.5-10539del ENSP00000465818.1:n.5-10539del
ENST00000591534.5:c.-12del ENSP00000467329.1:n.-12del
ENST00000591849.5:c.-98-24300del ENSP00000465347.1:n.-98-24300del
NM_007294.3:c.4516del , LRG_292t1:c.4516del NP_009225.1:p.Asp1506IlefsTer?
NM_007297.3:c.4375del NP_009228.2:p.Asp1459IlefsTer?
NM_007298.3:c.1204del NP_009229.2:p.Asp402IlefsTer?
NM_007299.3:c.1204del NP_009230.2:p.Asp402IlefsTer?
NM_007300.3:c.4579del NP_009231.2:p.Asp1527IlefsTer?
NR_027676.1:n.4652del
NM_007294.4:c.4516del MANE Select NP_009225.1:p.Asp1506IlefsTer?
NM_007297.4:c.4375del NP_009228.2:p.Asp1459IlefsTer?
NM_007299.4:c.1204del NP_009230.2:p.Asp402IlefsTer?
NM_007300.4:c.4579del NP_009231.2:p.Asp1527IlefsTer?
NR_027676.2:n.4693del