Canonical Allele Identifier: CA2260761064
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43045729G= , CM000679.2:g.43045729G= GRCh38
NC_000017.10:g.41197746G= , CM000679.1:g.41197746G= GRCh37
NC_000017.9:g.38451272G= NCBI36
NG_005905.2:g.172255C= , LRG_292:g.172255C=

Transcript Alleles

HGVS Amino-acid change
ENST00000461574.2:c.5538C= ENSP00000417241.2:p.Cys1846=
ENST00000470026.6:c.5541C= ENSP00000419274.2:p.Cys1847=
ENST00000473961.6:c.5415C= ENSP00000420201.2:p.Cys1805=
ENST00000476777.6:c.5535C= ENSP00000417554.2:p.Cys1845=
ENST00000477152.6:c.5463C= ENSP00000419988.2:p.Cys1821=
ENST00000478531.6:c.2229C= ENSP00000420412.2:p.Cys743=
ENST00000489037.2:c.5463C= ENSP00000420781.2:p.Cys1821=
ENST00000493919.6:c.2091C= ENSP00000418819.2:p.Cys697=
ENST00000494123.6:c.5541C= ENSP00000419103.2:p.Cys1847=
ENST00000497488.2:c.4653C= ENSP00000418986.2:p.Cys1551=
ENST00000618469.2:c.5541C= ENSP00000478114.2:p.Cys1847=
ENST00000634433.2:c.5418C= ENSP00000489431.2:p.Cys1806=
ENST00000644379.2:c.5607C= ENSP00000496570.2:p.Cys1869=
ENST00000644555.2:c.2091C= ENSP00000494614.2:p.Cys697=
ENST00000652672.2:c.5400C= ENSP00000498906.2:p.Cys1800=
ENST00000484087.6:c.2103C= ENSP00000419481.2:p.Cys701=
ENST00000700081.1:n.1424C=
ENST00000700082.1:n.905C=
ENST00000357654.9:c.5541C= MANE Select ENSP00000350283.3:p.Cys1847=
ENST00000471181.7:c.5604C= ENSP00000418960.2:p.Cys1868=
ENST00000644379.1:c.1928C=
ENST00000352993.7:c.2115C= ENSP00000312236.5:p.Cys705=
ENST00000357654.7:c.5541C= ENSP00000350283.3:p.Cys1847=
ENST00000461221.5:c.*5324C= ENSP00000418548.1:n.*5324C=
ENST00000468300.5:c.*55C= ENSP00000417148.1:n.*55C=
ENST00000471181.6:c.5604C= ENSP00000418960.2:p.Cys1868=
ENST00000491747.6:c.2229C= ENSP00000420705.2:p.Cys743=
ENST00000493795.5:c.5400C= ENSP00000418775.1:p.Cys1800=
ENST00000586385.5:c.471C= ENSP00000465818.1:p.Cys157=
ENST00000591534.5:c.1014C= ENSP00000467329.1:p.Cys338=
ENST00000591849.5:c.240C= ENSP00000465347.1:p.Cys80=
NM_007294.3:c.5541C= , LRG_292t1:c.5541C= NP_009225.1:p.Cys1847=
NM_007297.3:c.5400C= NP_009228.2:p.Cys1800=
NM_007298.3:c.2229C= NP_009229.2:p.Cys743=
NM_007299.3:c.*55C= NP_009230.2:n.*55C=
NM_007300.3:c.5604C= NP_009231.2:p.Cys1868=
NR_027676.1:n.5677C=
NM_007294.4:c.5541C= MANE Select NP_009225.1:p.Cys1847=
NM_007297.4:c.5400C= NP_009228.2:p.Cys1800=
NM_007299.4:c.*55C= NP_009230.2:n.*55C=
NM_007300.4:c.5604C= NP_009231.2:p.Cys1868=
NR_027676.2:n.5718C=