Canonical Allele Identifier: CA2260774514
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43074436A= , CM000679.2:g.43074436A= GRCh38
NC_000017.10:g.41226453A= , CM000679.1:g.41226453A= GRCh37
NC_000017.9:g.38479979A= NCBI36
NG_005905.2:g.143548T= , LRG_292:g.143548T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000461574.2:c.4567T= ENSP00000417241.2:p.Ser1523=
ENST00000470026.6:c.4570T= ENSP00000419274.2:p.Ser1524=
ENST00000473961.6:c.4444T= ENSP00000420201.2:p.Ser1482=
ENST00000476777.6:c.4564T= ENSP00000417554.2:p.Ser1522=
ENST00000477152.6:c.4492T= ENSP00000419988.2:p.Ser1498=
ENST00000478531.6:c.1258T= ENSP00000420412.2:p.Ser420=
ENST00000489037.2:c.4492T= ENSP00000420781.2:p.Ser1498=
ENST00000493919.6:c.1120T= ENSP00000418819.2:p.Ser374=
ENST00000494123.6:c.4570T= ENSP00000419103.2:p.Ser1524=
ENST00000497488.2:c.3682T= ENSP00000418986.2:p.Ser1228=
ENST00000618469.2:c.4570T= ENSP00000478114.2:p.Ser1524=
ENST00000634433.2:c.4447T= ENSP00000489431.2:p.Ser1483=
ENST00000644379.2:c.4636T= ENSP00000496570.2:p.Ser1546=
ENST00000644555.2:c.1120T= ENSP00000494614.2:p.Ser374=
ENST00000652672.2:c.4429T= ENSP00000498906.2:p.Ser1477=
ENST00000484087.6:c.1132T= ENSP00000419481.2:p.Ser378=
ENST00000700182.1:c.1177T= ENSP00000514849.1:p.Ser393=
ENST00000357654.9:c.4570T= MANE Select ENSP00000350283.3:p.Ser1524=
ENST00000471181.7:c.4633T= ENSP00000418960.2:p.Ser1545=
ENST00000644379.1:c.957T=
ENST00000352993.7:c.1144T= ENSP00000312236.5:p.Ser382=
ENST00000357654.7:c.4570T= ENSP00000350283.3:p.Ser1524=
ENST00000461221.5:c.*4353T= ENSP00000418548.1:n.*4353T=
ENST00000468300.5:c.1258T= ENSP00000417148.1:p.Ser420=
ENST00000471181.6:c.4633T= ENSP00000418960.2:p.Ser1545=
ENST00000478531.5:c.1258T= ENSP00000420412.1:p.Ser420=
ENST00000484087.5:c.883T= ENSP00000419481.1:p.Ser295=
ENST00000491747.6:c.1258T= ENSP00000420705.2:p.Ser420=
ENST00000493795.5:c.4429T= ENSP00000418775.1:p.Ser1477=
ENST00000493919.5:c.1120T= ENSP00000418819.1:p.Ser374=
ENST00000586385.5:c.5-10485T= ENSP00000465818.1:n.5-10485T=
ENST00000591534.5:c.43T= ENSP00000467329.1:p.Ser15=
ENST00000591849.5:c.-98-24246T= ENSP00000465347.1:n.-98-24246T=
NM_007294.3:c.4570T= , LRG_292t1:c.4570T= NP_009225.1:p.Ser1524=
NM_007297.3:c.4429T= NP_009228.2:p.Ser1477=
NM_007298.3:c.1258T= NP_009229.2:p.Ser420=
NM_007299.3:c.1258T= NP_009230.2:p.Ser420=
NM_007300.3:c.4633T= NP_009231.2:p.Ser1545=
NR_027676.1:n.4706T=
NM_007294.4:c.4570T= MANE Select NP_009225.1:p.Ser1524=
NM_007297.4:c.4429T= NP_009228.2:p.Ser1477=
NM_007299.4:c.1258T= NP_009230.2:p.Ser420=
NM_007300.4:c.4633T= NP_009231.2:p.Ser1545=
NR_027676.2:n.4747T=