Canonical Allele Identifier: CA2260763659

Gene: BRCA1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43051042G= , CM000679.2:g.43051042G=	GRCh38
NC_000017.10:g.41203059G= , CM000679.1:g.41203059G=	GRCh37
NC_000017.9:g.38456585G=	NCBI36
NG_005905.2:g.166942C= , LRG_292:g.166942C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461574.2:c.5329+21C=	ENSP00000417241.2:n.5329+21C=
ENST00000470026.6:c.5332+21C=	ENSP00000419274.2:n.5332+21C=
ENST00000473961.6:c.5206+21C=	ENSP00000420201.2:n.5206+21C=
ENST00000476777.6:c.5326+21C=	ENSP00000417554.2:n.5326+21C=
ENST00000477152.6:c.5254+21C=	ENSP00000419988.2:n.5254+21C=
ENST00000478531.6:c.2020+21C=	ENSP00000420412.2:n.2020+21C=
ENST00000489037.2:c.5254+21C=	ENSP00000420781.2:n.5254+21C=
ENST00000493919.6:c.1882+21C=	ENSP00000418819.2:n.1882+21C=
ENST00000494123.6:c.5332+21C=	ENSP00000419103.2:n.5332+21C=
ENST00000497488.2:c.4444+21C=	ENSP00000418986.2:n.4444+21C=
ENST00000618469.2:c.5332+21C=	ENSP00000478114.2:n.5332+21C=
ENST00000634433.2:c.5209+21C=	ENSP00000489431.2:n.5209+21C=
ENST00000644379.2:c.5398+21C=	ENSP00000496570.2:n.5398+21C=
ENST00000644555.2:c.1882+21C=	ENSP00000494614.2:n.1882+21C=
ENST00000652672.2:c.5191+21C=	ENSP00000498906.2:n.5191+21C=
ENST00000484087.6:c.1894+21C=	ENSP00000419481.2:n.1894+21C=
ENST00000357654.9:c.5332+21C= MANE Select	ENSP00000350283.3:n.5332+21C=
ENST00000471181.7:c.5395+21C=	ENSP00000418960.2:n.5395+21C=
ENST00000644379.1:c.1719+21C=
ENST00000352993.7:c.1906+21C=	ENSP00000312236.5:n.1906+21C=
ENST00000357654.7:c.5332+21C=	ENSP00000350283.3:n.5332+21C=
ENST00000461221.5:c.*5115+21C=	ENSP00000418548.1:n.*5115+21C=
ENST00000468300.5:c.2020+21C=	ENSP00000417148.1:n.2020+21C=
ENST00000471181.6:c.5395+21C=	ENSP00000418960.2:n.5395+21C=
ENST00000491747.6:c.2020+21C=	ENSP00000420705.2:n.2020+21C=
ENST00000493795.5:c.5191+21C=	ENSP00000418775.1:n.5191+21C=
ENST00000586385.5:c.262+21C=	ENSP00000465818.1:n.262+21C=
ENST00000591534.5:c.805+21C=	ENSP00000467329.1:n.805+21C=
ENST00000591849.5:c.-98-852C=	ENSP00000465347.1:n.-98-852C=
NM_007294.3:c.5332+21C= , LRG_292t1:c.5332+21C=	NP_009225.1:n.5332+21C=
NM_007297.3:c.5191+21C=	NP_009228.2:n.5191+21C=
NM_007298.3:c.2020+21C=	NP_009229.2:n.2020+21C=
NM_007299.3:c.2020+21C=	NP_009230.2:n.2020+21C=
NM_007300.3:c.5395+21C=	NP_009231.2:n.5395+21C=
NR_027676.1:n.5468+21C=
NM_007294.4:c.5332+21C= MANE Select	NP_009225.1:n.5332+21C=
NM_007297.4:c.5191+21C=	NP_009228.2:n.5191+21C=
NM_007299.4:c.2020+21C=	NP_009230.2:n.2020+21C=
NM_007300.4:c.5395+21C=	NP_009231.2:n.5395+21C=
NR_027676.2:n.5509+21C=