Canonical Allele Identifier: CA2260778792

Gene: BRCA1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43084241A= , CM000679.2:g.43084241A=	GRCh38
NC_000017.10:g.41236258A= , CM000679.1:g.41236258A=	GRCh37
NC_000017.9:g.38489784A=	NCBI36
NG_005905.2:g.133743T= , LRG_292:g.133743T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461574.2:c.4186-1666T=	ENSP00000417241.2:n.4186-1666T=
ENST00000470026.6:c.4186-1666T=	ENSP00000419274.2:n.4186-1666T=
ENST00000473961.6:c.4060-1666T=	ENSP00000420201.2:n.4060-1666T=
ENST00000476777.6:c.4183-1669T=	ENSP00000417554.2:n.4183-1669T=
ENST00000477152.6:c.4108-1666T=	ENSP00000419988.2:n.4108-1666T=
ENST00000478531.6:c.874-1666T=	ENSP00000420412.2:n.874-1666T=
ENST00000489037.2:c.4108-1666T=	ENSP00000420781.2:n.4108-1666T=
ENST00000493919.6:c.736-1666T=	ENSP00000418819.2:n.736-1666T=
ENST00000494123.6:c.4186-1666T=	ENSP00000419103.2:n.4186-1666T=
ENST00000497488.2:c.3298-1666T=	ENSP00000418986.2:n.3298-1666T=
ENST00000618469.2:c.4186-1666T=	ENSP00000478114.2:n.4186-1666T=
ENST00000634433.2:c.4063-1666T=	ENSP00000489431.2:n.4063-1666T=
ENST00000644379.2:c.4186-1666T=	ENSP00000496570.2:n.4186-1666T=
ENST00000644555.2:c.736-1666T=	ENSP00000494614.2:n.736-1666T=
ENST00000652672.2:c.4045-1666T=	ENSP00000498906.2:n.4045-1666T=
ENST00000484087.6:c.754-1669T=	ENSP00000419481.2:n.754-1669T=
ENST00000700182.1:c.796-1666T=	ENSP00000514849.1:n.796-1666T=
ENST00000357654.9:c.4186-1666T= MANE Select	ENSP00000350283.3:n.4186-1666T=
ENST00000471181.7:c.4186-1666T=	ENSP00000418960.2:n.4186-1666T=
ENST00000644379.1:c.507-1666T=
ENST00000352993.7:c.760-1666T=	ENSP00000312236.5:n.760-1666T=
ENST00000357654.7:c.4186-1666T=	ENSP00000350283.3:n.4186-1666T=
ENST00000461221.5:c.*3969-1666T=	ENSP00000418548.1:n.*3969-1666T=
ENST00000461574.1:c.480-1666T=
ENST00000468300.5:c.877-1666T=	ENSP00000417148.1:n.877-1666T=
ENST00000471181.6:c.4186-1666T=	ENSP00000418960.2:n.4186-1666T=
ENST00000478531.5:c.874-1666T=	ENSP00000420412.1:n.874-1666T=
ENST00000484087.5:c.499-1666T=	ENSP00000419481.1:n.499-1666T=
ENST00000487825.5:c.502-1666T=	ENSP00000418212.1:n.502-1666T=
ENST00000491747.6:c.877-1666T=	ENSP00000420705.2:n.877-1666T=
ENST00000493795.5:c.4045-1666T=	ENSP00000418775.1:n.4045-1666T=
ENST00000493919.5:c.736-1666T=	ENSP00000418819.1:n.736-1666T=
ENST00000586385.5:c.5-20290T=	ENSP00000465818.1:n.5-20290T=
ENST00000591534.5:c.-43-9720T=	ENSP00000467329.1:n.-43-9720T=
ENST00000591849.5:c.-98-34051T=	ENSP00000465347.1:n.-98-34051T=
NM_007294.3:c.4186-1666T= , LRG_292t1:c.4186-1666T=	NP_009225.1:n.4186-1666T=
NM_007297.3:c.4045-1666T=	NP_009228.2:n.4045-1666T=
NM_007298.3:c.877-1666T=	NP_009229.2:n.877-1666T=
NM_007299.3:c.877-1666T=	NP_009230.2:n.877-1666T=
NM_007300.3:c.4186-1666T=	NP_009231.2:n.4186-1666T=
NR_027676.1:n.4322-1666T=
NM_007294.4:c.4186-1666T= MANE Select	NP_009225.1:n.4186-1666T=
NM_007297.4:c.4045-1666T=	NP_009228.2:n.4045-1666T=
NM_007299.4:c.877-1666T=	NP_009230.2:n.877-1666T=
NM_007300.4:c.4186-1666T=	NP_009231.2:n.4186-1666T=
NR_027676.2:n.4363-1666T=