Canonical Allele Identifier: CA2260777987
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43082451G= , CM000679.2:g.43082451G= GRCh38
NC_000017.10:g.41234468G= , CM000679.1:g.41234468G= GRCh37
NC_000017.9:g.38487994G= NCBI36
NG_005905.2:g.135533C= , LRG_292:g.135533C=

Transcript Alleles

HGVS Amino-acid change
ENST00000461574.2:c.4310C= ENSP00000417241.2:p.Ser1437=
ENST00000470026.6:c.4310C= ENSP00000419274.2:p.Ser1437=
ENST00000473961.6:c.4184C= ENSP00000420201.2:p.Ser1395=
ENST00000476777.6:c.4304C= ENSP00000417554.2:p.Ser1435=
ENST00000477152.6:c.4232C= ENSP00000419988.2:p.Ser1411=
ENST00000478531.6:c.998C= ENSP00000420412.2:p.Ser333=
ENST00000489037.2:c.4232C= ENSP00000420781.2:p.Ser1411=
ENST00000493919.6:c.860C= ENSP00000418819.2:p.Ser287=
ENST00000494123.6:c.4310C= ENSP00000419103.2:p.Ser1437=
ENST00000497488.2:c.3422C= ENSP00000418986.2:p.Ser1141=
ENST00000618469.2:c.4310C= ENSP00000478114.2:p.Ser1437=
ENST00000634433.2:c.4187C= ENSP00000489431.2:p.Ser1396=
ENST00000644379.2:c.4310C= ENSP00000496570.2:p.Ser1437=
ENST00000644555.2:c.860C= ENSP00000494614.2:p.Ser287=
ENST00000652672.2:c.4169C= ENSP00000498906.2:p.Ser1390=
ENST00000484087.6:c.875C= ENSP00000419481.2:p.Ser292=
ENST00000700182.1:c.920C= ENSP00000514849.1:p.Ser307=
ENST00000357654.9:c.4310C= MANE Select ENSP00000350283.3:p.Ser1437=
ENST00000471181.7:c.4310C= ENSP00000418960.2:p.Ser1437=
ENST00000644379.1:c.631C=
ENST00000352993.7:c.884C= ENSP00000312236.5:p.Ser295=
ENST00000357654.7:c.4310C= ENSP00000350283.3:p.Ser1437=
ENST00000461221.5:c.*4093C= ENSP00000418548.1:n.*4093C=
ENST00000461574.1:c.604C=
ENST00000468300.5:c.1001C= ENSP00000417148.1:p.Ser334=
ENST00000471181.6:c.4310C= ENSP00000418960.2:p.Ser1437=
ENST00000478531.5:c.998C= ENSP00000420412.1:p.Ser333=
ENST00000484087.5:c.623C= ENSP00000419481.1:p.Ser208=
ENST00000487825.5:c.626C= ENSP00000418212.1:p.Ser209=
ENST00000491747.6:c.1001C= ENSP00000420705.2:p.Ser334=
ENST00000493795.5:c.4169C= ENSP00000418775.1:p.Ser1390=
ENST00000493919.5:c.860C= ENSP00000418819.1:p.Ser287=
ENST00000586385.5:c.5-18500C= ENSP00000465818.1:n.5-18500C=
ENST00000591534.5:c.-43-7930C= ENSP00000467329.1:n.-43-7930C=
ENST00000591849.5:c.-98-32261C= ENSP00000465347.1:n.-98-32261C=
ENST00000621897.1:n.204C=
NM_007294.3:c.4310C= , LRG_292t1:c.4310C= NP_009225.1:p.Ser1437=
NM_007297.3:c.4169C= NP_009228.2:p.Ser1390=
NM_007298.3:c.1001C= NP_009229.2:p.Ser334=
NM_007299.3:c.1001C= NP_009230.2:p.Ser334=
NM_007300.3:c.4310C= NP_009231.2:p.Ser1437=
NR_027676.1:n.4446C=
NM_007294.4:c.4310C= MANE Select NP_009225.1:p.Ser1437=
NM_007297.4:c.4169C= NP_009228.2:p.Ser1390=
NM_007299.4:c.1001C= NP_009230.2:p.Ser334=
NM_007300.4:c.4310C= NP_009231.2:p.Ser1437=
NR_027676.2:n.4487C=