Canonical Allele Identifier: CA10593243

Gene: BRCA1

Linked Data

• dbSNP Id: rs2154157344
• MyVariant Identifiers: chr17:g.41234540T>A (hg19) ; chr17:g.43082523T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43082523T>A , CM000679.2:g.43082523T>A	GRCh38
NC_000017.10:g.41234540T>A , CM000679.1:g.41234540T>A	GRCh37
NC_000017.9:g.38488066T>A	NCBI36
NG_005905.2:g.135461A>T , LRG_292:g.135461A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461574.2:c.4238A>T	ENSP00000417241.2:p.Glu1413Val
ENST00000470026.6:c.4238A>T	ENSP00000419274.2:p.Glu1413Val
ENST00000473961.6:c.4112A>T	ENSP00000420201.2:p.Glu1371Val
ENST00000476777.6:c.4232A>T	ENSP00000417554.2:p.Glu1411Val
ENST00000477152.6:c.4160A>T	ENSP00000419988.2:p.Glu1387Val
ENST00000478531.6:c.926A>T	ENSP00000420412.2:p.Glu309Val
ENST00000489037.2:c.4160A>T	ENSP00000420781.2:p.Glu1387Val
ENST00000493919.6:c.788A>T	ENSP00000418819.2:p.Glu263Val
ENST00000494123.6:c.4238A>T	ENSP00000419103.2:p.Glu1413Val
ENST00000497488.2:c.3350A>T	ENSP00000418986.2:p.Glu1117Val
ENST00000618469.2:c.4238A>T	ENSP00000478114.2:p.Glu1413Val
ENST00000634433.2:c.4115A>T	ENSP00000489431.2:p.Glu1372Val
ENST00000644379.2:c.4238A>T	ENSP00000496570.2:p.Glu1413Val
ENST00000644555.2:c.788A>T	ENSP00000494614.2:p.Glu263Val
ENST00000652672.2:c.4097A>T	ENSP00000498906.2:p.Glu1366Val
ENST00000484087.6:c.803A>T	ENSP00000419481.2:p.Glu268Val
ENST00000700182.1:c.848A>T	ENSP00000514849.1:p.Glu283Val
ENST00000357654.9:c.4238A>T MANE Select	ENSP00000350283.3:p.Glu1413Val
ENST00000471181.7:c.4238A>T	ENSP00000418960.2:p.Glu1413Val
ENST00000644379.1:c.559A>T
ENST00000352993.7:c.812A>T	ENSP00000312236.5:p.Glu271Val
ENST00000357654.7:c.4238A>T	ENSP00000350283.3:p.Glu1413Val
ENST00000461221.5:c.*4021A>T	ENSP00000418548.1:n.*4021A>T
ENST00000461574.1:c.532A>T
ENST00000468300.5:c.929A>T	ENSP00000417148.1:p.Glu310Val
ENST00000471181.6:c.4238A>T	ENSP00000418960.2:p.Glu1413Val
ENST00000478531.5:c.926A>T	ENSP00000420412.1:p.Glu309Val
ENST00000484087.5:c.551A>T	ENSP00000419481.1:p.Glu184Val
ENST00000487825.5:c.554A>T	ENSP00000418212.1:p.Glu185Val
ENST00000491747.6:c.929A>T	ENSP00000420705.2:p.Glu310Val
ENST00000493795.5:c.4097A>T	ENSP00000418775.1:p.Glu1366Val
ENST00000493919.5:c.788A>T	ENSP00000418819.1:p.Glu263Val
ENST00000586385.5:c.5-18572A>T	ENSP00000465818.1:n.5-18572A>T
ENST00000591534.5:c.-43-8002A>T	ENSP00000467329.1:n.-43-8002A>T
ENST00000591849.5:c.-98-32333A>T	ENSP00000465347.1:n.-98-32333A>T
ENST00000621897.1:n.132A>T
NM_007294.3:c.4238A>T , LRG_292t1:c.4238A>T	NP_009225.1:p.Glu1413Val
NM_007297.3:c.4097A>T	NP_009228.2:p.Glu1366Val
NM_007298.3:c.929A>T	NP_009229.2:p.Glu310Val
NM_007299.3:c.929A>T	NP_009230.2:p.Glu310Val
NM_007300.3:c.4238A>T	NP_009231.2:p.Glu1413Val
NR_027676.1:n.4374A>T
NM_007294.4:c.4238A>T MANE Select	NP_009225.1:p.Glu1413Val
NM_007297.4:c.4097A>T	NP_009228.2:p.Glu1366Val
NM_007299.4:c.929A>T	NP_009230.2:p.Glu310Val
NM_007300.4:c.4238A>T	NP_009231.2:p.Glu1413Val
NR_027676.2:n.4415A>T