Canonical Allele Identifier: CA2260790375

Gene: BRCA1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43104129G= , CM000679.2:g.43104129G=	GRCh38
NC_000017.10:g.41256146G= , CM000679.1:g.41256146G=	GRCh37
NC_000017.9:g.38509672G=	NCBI36
NG_005905.2:g.113855C= , LRG_292:g.113855C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354071.8:n.498C=
ENST00000461574.2:c.434C=	ENSP00000417241.2:p.Pro145=
ENST00000470026.6:c.434C=	ENSP00000419274.2:p.Pro145=
ENST00000473961.6:c.434C=	ENSP00000420201.2:p.Pro145=
ENST00000476777.6:c.434C=	ENSP00000417554.2:p.Pro145=
ENST00000477152.6:c.356C=	ENSP00000419988.2:p.Pro119=
ENST00000478531.6:c.434C=	ENSP00000420412.2:p.Pro145=
ENST00000489037.2:c.356C=	ENSP00000420781.2:p.Pro119=
ENST00000493919.6:c.293C=	ENSP00000418819.2:p.Pro98=
ENST00000494123.6:c.434C=	ENSP00000419103.2:p.Pro145=
ENST00000497488.2:c.-218-9269C=	ENSP00000418986.2:n.-218-9269C=
ENST00000618469.2:c.434C=	ENSP00000478114.2:p.Pro145=
ENST00000634433.2:c.434C=	ENSP00000489431.2:p.Pro145=
ENST00000644379.2:c.434C=	ENSP00000496570.2:p.Pro145=
ENST00000644555.2:c.293C=	ENSP00000494614.2:p.Pro98=
ENST00000652672.2:c.293C=	ENSP00000498906.2:p.Pro98=
ENST00000484087.6:c.434C=	ENSP00000419481.2:p.Pro145=
ENST00000700182.1:c.356C=	ENSP00000514849.1:p.Pro119=
ENST00000700183.1:c.*348C=	ENSP00000514850.1:n.*348C=
ENST00000700184.1:n.677C=
ENST00000357654.9:c.434C= MANE Select	ENSP00000350283.3:p.Pro145=
ENST00000471181.7:c.434C=	ENSP00000418960.2:p.Pro145=
ENST00000642945.1:c.*308C=	ENSP00000495897.1:n.*308C=
ENST00000652672.1:c.293C=	ENSP00000498906.1:p.Pro98=
ENST00000352993.7:c.434C=	ENSP00000312236.5:p.Pro145=
ENST00000354071.7:c.434C=	ENSP00000326002.7:p.Pro145=
ENST00000357654.7:c.434C=	ENSP00000350283.3:p.Pro145=
ENST00000461221.5:c.*220C=	ENSP00000418548.1:n.*220C=
ENST00000461798.5:c.*220C=	ENSP00000417988.1:n.*220C=
ENST00000468300.5:c.434C=	ENSP00000417148.1:p.Pro145=
ENST00000470026.5:c.434C=	ENSP00000419274.1:p.Pro145=
ENST00000471181.6:c.434C=	ENSP00000418960.2:p.Pro145=
ENST00000473961.5:c.157C=
ENST00000476777.5:c.434C=	ENSP00000417554.1:p.Pro145=
ENST00000477152.5:c.356C=	ENSP00000419988.1:p.Pro119=
ENST00000478531.5:c.434C=	ENSP00000420412.1:p.Pro145=
ENST00000484087.5:c.182C=	ENSP00000419481.1:p.Pro61=
ENST00000487825.5:c.182C=	ENSP00000418212.1:p.Pro61=
ENST00000491747.6:c.434C=	ENSP00000420705.2:p.Pro145=
ENST00000492859.5:c.*370C=	ENSP00000420253.1:n.*370C=
ENST00000493795.5:c.293C=	ENSP00000418775.1:p.Pro98=
ENST00000493919.5:c.293C=	ENSP00000418819.1:p.Pro98=
ENST00000494123.5:c.434C=	ENSP00000419103.1:p.Pro145=
ENST00000497488.1:c.-218-9269C=	ENSP00000418986.1:n.-218-9269C=
ENST00000586385.5:c.4+21053C=	ENSP00000465818.1:n.4+21053C=
ENST00000591534.5:c.-44+21142C=	ENSP00000467329.1:n.-44+21142C=
ENST00000591849.5:c.-99+21142C=	ENSP00000465347.1:n.-99+21142C=
ENST00000634433.1:c.434C=	ENSP00000489431.1:p.Pro145=
NM_007294.3:c.434C= , LRG_292t1:c.434C=	NP_009225.1:p.Pro145=
NM_007297.3:c.293C=	NP_009228.2:p.Pro98=
NM_007298.3:c.434C=	NP_009229.2:p.Pro145=
NM_007299.3:c.434C=	NP_009230.2:p.Pro145=
NM_007300.3:c.434C=	NP_009231.2:p.Pro145=
NR_027676.1:n.573C=
NM_007294.4:c.434C= MANE Select	NP_009225.1:p.Pro145=
NM_007297.4:c.293C=	NP_009228.2:p.Pro98=
NM_007299.4:c.434C=	NP_009230.2:p.Pro145=
NM_007300.4:c.434C=	NP_009231.2:p.Pro145=
NR_027676.2:n.614C=