Canonical Allele Identifier: CA10586665

Gene: BRCA1

Linked Data

• ClinVar Variation Id: 254380
• ClinVar RCV Id: RCV000240999 ; RCV001026872 ; RCV001207336 ; RCV001727656
• dbSNP Id: rs886037979
• MyVariant Identifiers: chr17:g.41246764G>A (hg19) ; chr17:g.43094747G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43094747G>A , CM000679.2:g.43094747G>A	GRCh38
NC_000017.10:g.41246764G>A , CM000679.1:g.41246764G>A	GRCh37
NC_000017.9:g.38500290G>A	NCBI36
NG_005905.2:g.123237C>T , LRG_292:g.123237C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354071.8:n.848C>T
ENST00000461574.2:c.784C>T	ENSP00000417241.2:p.Gln262Ter
ENST00000470026.6:c.784C>T	ENSP00000419274.2:p.Gln262Ter
ENST00000473961.6:c.658C>T	ENSP00000420201.2:p.Gln220Ter
ENST00000476777.6:c.781C>T	ENSP00000417554.2:p.Gln261Ter
ENST00000477152.6:c.706C>T	ENSP00000419988.2:p.Gln236Ter
ENST00000478531.6:c.781C>T	ENSP00000420412.2:p.Gln261Ter
ENST00000489037.2:c.706C>T	ENSP00000420781.2:p.Gln236Ter
ENST00000493919.6:c.643C>T	ENSP00000418819.2:p.Gln215Ter
ENST00000494123.6:c.784C>T	ENSP00000419103.2:p.Gln262Ter
ENST00000497488.2:c.-105C>T	ENSP00000418986.2:n.-105C>T
ENST00000618469.2:c.784C>T	ENSP00000478114.2:p.Gln262Ter
ENST00000634433.2:c.661C>T	ENSP00000489431.2:p.Gln221Ter
ENST00000644379.2:c.784C>T	ENSP00000496570.2:p.Gln262Ter
ENST00000644555.2:c.643C>T	ENSP00000494614.2:p.Gln215Ter
ENST00000652672.2:c.643C>T	ENSP00000498906.2:p.Gln215Ter
ENST00000484087.6:c.661C>T	ENSP00000419481.2:p.Gln221Ter
ENST00000700182.1:c.703C>T	ENSP00000514849.1:p.Gln235Ter
ENST00000700183.1:c.*792C>T	ENSP00000514850.1:n.*792C>T
ENST00000357654.9:c.784C>T MANE Select	ENSP00000350283.3:p.Gln262Ter
ENST00000471181.7:c.784C>T	ENSP00000418960.2:p.Gln262Ter
ENST00000642945.1:c.*658C>T	ENSP00000495897.1:n.*658C>T
ENST00000652672.1:c.643C>T	ENSP00000498906.1:p.Gln215Ter
ENST00000352993.7:c.670+1099C>T	ENSP00000312236.5:n.670+1099C>T
ENST00000354071.7:c.784C>T	ENSP00000326002.7:p.Gln262Ter
ENST00000357654.7:c.784C>T	ENSP00000350283.3:p.Gln262Ter
ENST00000412061.3:c.135C>T
ENST00000461221.5:c.*567C>T	ENSP00000418548.1:n.*567C>T
ENST00000468300.5:c.784C>T	ENSP00000417148.1:p.Gln262Ter
ENST00000470026.5:c.784C>T	ENSP00000419274.1:p.Gln262Ter
ENST00000471181.6:c.784C>T	ENSP00000418960.2:p.Gln262Ter
ENST00000473961.5:c.381C>T
ENST00000477152.5:c.706C>T	ENSP00000419988.1:p.Gln236Ter
ENST00000478531.5:c.781C>T	ENSP00000420412.1:p.Gln261Ter
ENST00000484087.5:c.406C>T	ENSP00000419481.1:p.Gln136Ter
ENST00000487825.5:c.409C>T	ENSP00000418212.1:p.Gln137Ter
ENST00000491747.6:c.784C>T	ENSP00000420705.2:p.Gln262Ter
ENST00000492859.5:c.*720C>T	ENSP00000420253.1:n.*720C>T
ENST00000493795.5:c.643C>T	ENSP00000418775.1:p.Gln215Ter
ENST00000493919.5:c.643C>T	ENSP00000418819.1:p.Gln215Ter
ENST00000494123.5:c.784C>T	ENSP00000419103.1:p.Gln262Ter
ENST00000497488.1:c.-105C>T	ENSP00000418986.1:n.-105C>T
ENST00000586385.5:c.4+30435C>T	ENSP00000465818.1:n.4+30435C>T
ENST00000591534.5:c.-43-20226C>T	ENSP00000467329.1:n.-43-20226C>T
ENST00000591849.5:c.-99+30524C>T	ENSP00000465347.1:n.-99+30524C>T
ENST00000634433.1:c.661C>T	ENSP00000489431.1:p.Gln221Ter
NM_007294.3:c.784C>T , LRG_292t1:c.784C>T	NP_009225.1:p.Gln262Ter
NM_007297.3:c.643C>T	NP_009228.2:p.Gln215Ter
NM_007298.3:c.784C>T	NP_009229.2:p.Gln262Ter
NM_007299.3:c.784C>T	NP_009230.2:p.Gln262Ter
NM_007300.3:c.784C>T	NP_009231.2:p.Gln262Ter
NR_027676.1:n.920C>T
NM_007294.4:c.784C>T MANE Select	NP_009225.1:p.Gln262Ter
NM_007297.4:c.643C>T	NP_009228.2:p.Gln215Ter
NM_007299.4:c.784C>T	NP_009230.2:p.Gln262Ter
NM_007300.4:c.784C>T	NP_009231.2:p.Gln262Ter
NR_027676.2:n.961C>T