Canonical Allele Identifier: CA290815943

Gene: BRCA1

Linked Data

• dbSNP Id: rs9896925
• MyVariant Identifiers: chr17:g.41198675G>A (hg19) ; chr17:g.43046658G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43046658G>A , CM000679.2:g.43046658G>A	GRCh38
NC_000017.10:g.41198675G>A , CM000679.1:g.41198675G>A	GRCh37
NC_000017.9:g.38452201G>A	NCBI36
NG_005905.2:g.171326C>T , LRG_292:g.171326C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000461574.2:c.5465-856C>T	ENSP00000417241.2:n.5465-856C>T
ENST00000470026.6:c.5468-856C>T	ENSP00000419274.2:n.5468-856C>T
ENST00000473961.6:c.5342-856C>T	ENSP00000420201.2:n.5342-856C>T
ENST00000476777.6:c.5462-856C>T	ENSP00000417554.2:n.5462-856C>T
ENST00000477152.6:c.5390-856C>T	ENSP00000419988.2:n.5390-856C>T
ENST00000478531.6:c.2156-856C>T	ENSP00000420412.2:n.2156-856C>T
ENST00000489037.2:c.5390-856C>T	ENSP00000420781.2:n.5390-856C>T
ENST00000493919.6:c.2018-856C>T	ENSP00000418819.2:n.2018-856C>T
ENST00000494123.6:c.5468-856C>T	ENSP00000419103.2:n.5468-856C>T
ENST00000497488.2:c.4580-856C>T	ENSP00000418986.2:n.4580-856C>T
ENST00000618469.2:c.5468-856C>T	ENSP00000478114.2:n.5468-856C>T
ENST00000634433.2:c.5345-856C>T	ENSP00000489431.2:n.5345-856C>T
ENST00000644379.2:c.5534-856C>T	ENSP00000496570.2:n.5534-856C>T
ENST00000644555.2:c.2018-856C>T	ENSP00000494614.2:n.2018-856C>T
ENST00000652672.2:c.5327-856C>T	ENSP00000498906.2:n.5327-856C>T
ENST00000484087.6:c.2030-856C>T	ENSP00000419481.2:n.2030-856C>T
ENST00000700081.1:n.1351-856C>T
ENST00000700082.1:n.832-856C>T
ENST00000357654.9:c.5468-856C>T MANE Select	ENSP00000350283.3:n.5468-856C>T
ENST00000471181.7:c.5531-856C>T	ENSP00000418960.2:n.5531-856C>T
ENST00000644379.1:c.1855-856C>T
ENST00000352993.7:c.2042-856C>T	ENSP00000312236.5:n.2042-856C>T
ENST00000357654.7:c.5468-856C>T	ENSP00000350283.3:n.5468-856C>T
ENST00000461221.5:c.*5251-856C>T	ENSP00000418548.1:n.*5251-856C>T
ENST00000468300.5:c.2082-856C>T	ENSP00000417148.1:n.2082-856C>T
ENST00000471181.6:c.5531-856C>T	ENSP00000418960.2:n.5531-856C>T
ENST00000491747.6:c.2156-856C>T	ENSP00000420705.2:n.2156-856C>T
ENST00000493795.5:c.5327-856C>T	ENSP00000418775.1:n.5327-856C>T
ENST00000586385.5:c.398-856C>T	ENSP00000465818.1:n.398-856C>T
ENST00000591534.5:c.941-856C>T	ENSP00000467329.1:n.941-856C>T
ENST00000591849.5:c.167-856C>T	ENSP00000465347.1:n.167-856C>T
NM_007294.3:c.5468-856C>T , LRG_292t1:c.5468-856C>T	NP_009225.1:n.5468-856C>T
NM_007297.3:c.5327-856C>T	NP_009228.2:n.5327-856C>T
NM_007298.3:c.2156-856C>T	NP_009229.2:n.2156-856C>T
NM_007299.3:c.2082-856C>T	NP_009230.2:n.2082-856C>T
NM_007300.3:c.5531-856C>T	NP_009231.2:n.5531-856C>T
NR_027676.1:n.5604-856C>T
NM_007294.4:c.5468-856C>T MANE Select	NP_009225.1:n.5468-856C>T
NM_007297.4:c.5327-856C>T	NP_009228.2:n.5327-856C>T
NM_007299.4:c.2082-856C>T	NP_009230.2:n.2082-856C>T
NM_007300.4:c.5531-856C>T	NP_009231.2:n.5531-856C>T
NR_027676.2:n.5645-856C>T