Canonical Allele Identifier: CA10592476

Gene: BRCA1

Linked Data

• dbSNP Id: rs80356885
• MyVariant Identifiers: chr17:g.41226499C>G (hg19) ; chr17:g.43074482C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43074482C>G , CM000679.2:g.43074482C>G	GRCh38
NC_000017.10:g.41226499C>G , CM000679.1:g.41226499C>G	GRCh37
NC_000017.9:g.38480025C>G	NCBI36
NG_005905.2:g.143502G>C , LRG_292:g.143502G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000461574.2:c.4521G>C	ENSP00000417241.2:p.Trp1507Cys
ENST00000470026.6:c.4524G>C	ENSP00000419274.2:p.Trp1508Cys
ENST00000473961.6:c.4398G>C	ENSP00000420201.2:p.Trp1466Cys
ENST00000476777.6:c.4518G>C	ENSP00000417554.2:p.Trp1506Cys
ENST00000477152.6:c.4446G>C	ENSP00000419988.2:p.Trp1482Cys
ENST00000478531.6:c.1212G>C	ENSP00000420412.2:p.Trp404Cys
ENST00000489037.2:c.4446G>C	ENSP00000420781.2:p.Trp1482Cys
ENST00000493919.6:c.1074G>C	ENSP00000418819.2:p.Trp358Cys
ENST00000494123.6:c.4524G>C	ENSP00000419103.2:p.Trp1508Cys
ENST00000497488.2:c.3636G>C	ENSP00000418986.2:p.Trp1212Cys
ENST00000618469.2:c.4524G>C	ENSP00000478114.2:p.Trp1508Cys
ENST00000634433.2:c.4401G>C	ENSP00000489431.2:p.Trp1467Cys
ENST00000644379.2:c.4590G>C	ENSP00000496570.2:p.Trp1530Cys
ENST00000644555.2:c.1074G>C	ENSP00000494614.2:p.Trp358Cys
ENST00000652672.2:c.4383G>C	ENSP00000498906.2:p.Trp1461Cys
ENST00000484087.6:c.1086G>C	ENSP00000419481.2:p.Trp362Cys
ENST00000700182.1:c.1131G>C	ENSP00000514849.1:p.Trp377Cys
ENST00000357654.9:c.4524G>C MANE Select	ENSP00000350283.3:p.Trp1508Cys
ENST00000471181.7:c.4587G>C	ENSP00000418960.2:p.Trp1529Cys
ENST00000644379.1:c.911G>C
ENST00000352993.7:c.1098G>C	ENSP00000312236.5:p.Trp366Cys
ENST00000357654.7:c.4524G>C	ENSP00000350283.3:p.Trp1508Cys
ENST00000461221.5:c.*4307G>C	ENSP00000418548.1:n.*4307G>C
ENST00000468300.5:c.1212G>C	ENSP00000417148.1:p.Trp404Cys
ENST00000471181.6:c.4587G>C	ENSP00000418960.2:p.Trp1529Cys
ENST00000478531.5:c.1212G>C	ENSP00000420412.1:p.Trp404Cys
ENST00000484087.5:c.837G>C	ENSP00000419481.1:p.Trp279Cys
ENST00000491747.6:c.1212G>C	ENSP00000420705.2:p.Trp404Cys
ENST00000493795.5:c.4383G>C	ENSP00000418775.1:p.Trp1461Cys
ENST00000493919.5:c.1074G>C	ENSP00000418819.1:p.Trp358Cys
ENST00000586385.5:c.5-10531G>C	ENSP00000465818.1:n.5-10531G>C
ENST00000591534.5:c.-4G>C	ENSP00000467329.1:n.-4G>C
ENST00000591849.5:c.-98-24292G>C	ENSP00000465347.1:n.-98-24292G>C
NM_007294.3:c.4524G>C , LRG_292t1:c.4524G>C	NP_009225.1:p.Trp1508Cys
NM_007297.3:c.4383G>C	NP_009228.2:p.Trp1461Cys
NM_007298.3:c.1212G>C	NP_009229.2:p.Trp404Cys
NM_007299.3:c.1212G>C	NP_009230.2:p.Trp404Cys
NM_007300.3:c.4587G>C	NP_009231.2:p.Trp1529Cys
NR_027676.1:n.4660G>C
NM_007294.4:c.4524G>C MANE Select	NP_009225.1:p.Trp1508Cys
NM_007297.4:c.4383G>C	NP_009228.2:p.Trp1461Cys
NM_007299.4:c.1212G>C	NP_009230.2:p.Trp404Cys
NM_007300.4:c.4587G>C	NP_009231.2:p.Trp1529Cys
NR_027676.2:n.4701G>C