Canonical Allele Identifier: CA10592170

Gene: BRCA1

Linked Data

• dbSNP Id: rs869320779
• MyVariant Identifiers: chr17:g.41226353T>A (hg19) ; chr17:g.43074336T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43074336T>A , CM000679.2:g.43074336T>A	GRCh38
NC_000017.10:g.41226353T>A , CM000679.1:g.41226353T>A	GRCh37
NC_000017.9:g.38479879T>A	NCBI36
NG_005905.2:g.143648A>T , LRG_292:g.143648A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000461574.2:c.4667A>T	ENSP00000417241.2:p.Asp1556Val
ENST00000470026.6:c.4670A>T	ENSP00000419274.2:p.Asp1557Val
ENST00000473961.6:c.4544A>T	ENSP00000420201.2:p.Asp1515Val
ENST00000476777.6:c.4664A>T	ENSP00000417554.2:p.Asp1555Val
ENST00000477152.6:c.4592A>T	ENSP00000419988.2:p.Asp1531Val
ENST00000478531.6:c.1358A>T	ENSP00000420412.2:p.Asp453Val
ENST00000489037.2:c.4592A>T	ENSP00000420781.2:p.Asp1531Val
ENST00000493919.6:c.1220A>T	ENSP00000418819.2:p.Asp407Val
ENST00000494123.6:c.4670A>T	ENSP00000419103.2:p.Asp1557Val
ENST00000497488.2:c.3782A>T	ENSP00000418986.2:p.Asp1261Val
ENST00000618469.2:c.4670A>T	ENSP00000478114.2:p.Asp1557Val
ENST00000634433.2:c.4547A>T	ENSP00000489431.2:p.Asp1516Val
ENST00000644379.2:c.4736A>T	ENSP00000496570.2:p.Asp1579Val
ENST00000644555.2:c.1220A>T	ENSP00000494614.2:p.Asp407Val
ENST00000652672.2:c.4529A>T	ENSP00000498906.2:p.Asp1510Val
ENST00000484087.6:c.1232A>T	ENSP00000419481.2:p.Asp411Val
ENST00000700182.1:c.1277A>T	ENSP00000514849.1:p.Asp426Val
ENST00000357654.9:c.4670A>T MANE Select	ENSP00000350283.3:p.Asp1557Val
ENST00000471181.7:c.4733A>T	ENSP00000418960.2:p.Asp1578Val
ENST00000644379.1:c.1057A>T
ENST00000352993.7:c.1244A>T	ENSP00000312236.5:p.Asp415Val
ENST00000357654.7:c.4670A>T	ENSP00000350283.3:p.Asp1557Val
ENST00000461221.5:c.*4453A>T	ENSP00000418548.1:n.*4453A>T
ENST00000468300.5:c.1358A>T	ENSP00000417148.1:p.Asp453Val
ENST00000471181.6:c.4733A>T	ENSP00000418960.2:p.Asp1578Val
ENST00000478531.5:c.1358A>T	ENSP00000420412.1:p.Asp453Val
ENST00000484087.5:c.983A>T	ENSP00000419481.1:p.Asp328Val
ENST00000491747.6:c.1358A>T	ENSP00000420705.2:p.Asp453Val
ENST00000493795.5:c.4529A>T	ENSP00000418775.1:p.Asp1510Val
ENST00000493919.5:c.1220A>T	ENSP00000418819.1:p.Asp407Val
ENST00000586385.5:c.5-10385A>T	ENSP00000465818.1:n.5-10385A>T
ENST00000591534.5:c.143A>T	ENSP00000467329.1:p.Asp48Val
ENST00000591849.5:c.-98-24146A>T	ENSP00000465347.1:n.-98-24146A>T
NM_007294.3:c.4670A>T , LRG_292t1:c.4670A>T	NP_009225.1:p.Asp1557Val
NM_007297.3:c.4529A>T	NP_009228.2:p.Asp1510Val
NM_007298.3:c.1358A>T	NP_009229.2:p.Asp453Val
NM_007299.3:c.1358A>T	NP_009230.2:p.Asp453Val
NM_007300.3:c.4733A>T	NP_009231.2:p.Asp1578Val
NR_027676.1:n.4806A>T
NM_007294.4:c.4670A>T MANE Select	NP_009225.1:p.Asp1557Val
NM_007297.4:c.4529A>T	NP_009228.2:p.Asp1510Val
NM_007299.4:c.1358A>T	NP_009230.2:p.Asp453Val
NM_007300.4:c.4733A>T	NP_009231.2:p.Asp1578Val
NR_027676.2:n.4847A>T