Canonical Allele Identifier: CA2260777967

Gene: BRCA1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43082426T= , CM000679.2:g.43082426T=	GRCh38
NC_000017.10:g.41234443T= , CM000679.1:g.41234443T=	GRCh37
NC_000017.9:g.38487969T=	NCBI36
NG_005905.2:g.135558A= , LRG_292:g.135558A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461574.2:c.4335A=	ENSP00000417241.2:p.Pro1445=
ENST00000470026.6:c.4335A=	ENSP00000419274.2:p.Pro1445=
ENST00000473961.6:c.4209A=	ENSP00000420201.2:p.Pro1403=
ENST00000476777.6:c.4329A=	ENSP00000417554.2:p.Pro1443=
ENST00000477152.6:c.4257A=	ENSP00000419988.2:p.Pro1419=
ENST00000478531.6:c.1023A=	ENSP00000420412.2:p.Pro341=
ENST00000489037.2:c.4257A=	ENSP00000420781.2:p.Pro1419=
ENST00000493919.6:c.885A=	ENSP00000418819.2:p.Pro295=
ENST00000494123.6:c.4335A=	ENSP00000419103.2:p.Pro1445=
ENST00000497488.2:c.3447A=	ENSP00000418986.2:p.Pro1149=
ENST00000618469.2:c.4335A=	ENSP00000478114.2:p.Pro1445=
ENST00000634433.2:c.4212A=	ENSP00000489431.2:p.Pro1404=
ENST00000644379.2:c.4335A=	ENSP00000496570.2:p.Pro1445=
ENST00000644555.2:c.885A=	ENSP00000494614.2:p.Pro295=
ENST00000652672.2:c.4194A=	ENSP00000498906.2:p.Pro1398=
ENST00000484087.6:c.900A=	ENSP00000419481.2:p.Pro300=
ENST00000700182.1:c.945A=	ENSP00000514849.1:p.Pro315=
ENST00000357654.9:c.4335A= MANE Select	ENSP00000350283.3:p.Pro1445=
ENST00000471181.7:c.4335A=	ENSP00000418960.2:p.Pro1445=
ENST00000644379.1:c.656A=
ENST00000352993.7:c.909A=	ENSP00000312236.5:p.Pro303=
ENST00000357654.7:c.4335A=	ENSP00000350283.3:p.Pro1445=
ENST00000461221.5:c.*4118A=	ENSP00000418548.1:n.*4118A=
ENST00000461574.1:c.629A=
ENST00000468300.5:c.1026A=	ENSP00000417148.1:p.Pro342=
ENST00000471181.6:c.4335A=	ENSP00000418960.2:p.Pro1445=
ENST00000478531.5:c.1023A=	ENSP00000420412.1:p.Pro341=
ENST00000484087.5:c.648A=	ENSP00000419481.1:p.Pro216=
ENST00000487825.5:c.651A=	ENSP00000418212.1:p.Pro217=
ENST00000491747.6:c.1026A=	ENSP00000420705.2:p.Pro342=
ENST00000493795.5:c.4194A=	ENSP00000418775.1:p.Pro1398=
ENST00000493919.5:c.885A=	ENSP00000418819.1:p.Pro295=
ENST00000586385.5:c.5-18475A=	ENSP00000465818.1:n.5-18475A=
ENST00000591534.5:c.-43-7905A=	ENSP00000467329.1:n.-43-7905A=
ENST00000591849.5:c.-98-32236A=	ENSP00000465347.1:n.-98-32236A=
ENST00000621897.1:n.229A=
NM_007294.3:c.4335A= , LRG_292t1:c.4335A=	NP_009225.1:p.Pro1445=
NM_007297.3:c.4194A=	NP_009228.2:p.Pro1398=
NM_007298.3:c.1026A=	NP_009229.2:p.Pro342=
NM_007299.3:c.1026A=	NP_009230.2:p.Pro342=
NM_007300.3:c.4335A=	NP_009231.2:p.Pro1445=
NR_027676.1:n.4471A=
NM_007294.4:c.4335A= MANE Select	NP_009225.1:p.Pro1445=
NM_007297.4:c.4194A=	NP_009228.2:p.Pro1398=
NM_007299.4:c.1026A=	NP_009230.2:p.Pro342=
NM_007300.4:c.4335A=	NP_009231.2:p.Pro1445=
NR_027676.2:n.4512A=