Canonical Allele Identifier: CA10592616

Gene: BRCA1

Linked Data

• MyVariant Identifiers: chr17:g.41228530T>A (hg19) ; chr17:g.43076513T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43076513T>A , CM000679.2:g.43076513T>A	GRCh38
NC_000017.10:g.41228530T>A , CM000679.1:g.41228530T>A	GRCh37
NC_000017.9:g.38482056T>A	NCBI36
NG_005905.2:g.141471A>T , LRG_292:g.141471A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000461574.2:c.4456A>T	ENSP00000417241.2:p.Lys1486Ter
ENST00000470026.6:c.4459A>T	ENSP00000419274.2:p.Lys1487Ter
ENST00000473961.6:c.4333A>T	ENSP00000420201.2:p.Lys1445Ter
ENST00000476777.6:c.4453A>T	ENSP00000417554.2:p.Lys1485Ter
ENST00000477152.6:c.4381A>T	ENSP00000419988.2:p.Lys1461Ter
ENST00000478531.6:c.1147A>T	ENSP00000420412.2:p.Lys383Ter
ENST00000489037.2:c.4381A>T	ENSP00000420781.2:p.Lys1461Ter
ENST00000493919.6:c.1009A>T	ENSP00000418819.2:p.Lys337Ter
ENST00000494123.6:c.4459A>T	ENSP00000419103.2:p.Lys1487Ter
ENST00000497488.2:c.3571A>T	ENSP00000418986.2:p.Lys1191Ter
ENST00000618469.2:c.4459A>T	ENSP00000478114.2:p.Lys1487Ter
ENST00000634433.2:c.4336A>T	ENSP00000489431.2:p.Lys1446Ter
ENST00000644379.2:c.4525A>T	ENSP00000496570.2:p.Lys1509Ter
ENST00000644555.2:c.1009A>T	ENSP00000494614.2:p.Lys337Ter
ENST00000652672.2:c.4318A>T	ENSP00000498906.2:p.Lys1440Ter
ENST00000484087.6:c.1021A>T	ENSP00000419481.2:p.Lys341Ter
ENST00000700182.1:c.1066A>T	ENSP00000514849.1:p.Lys356Ter
ENST00000357654.9:c.4459A>T MANE Select	ENSP00000350283.3:p.Lys1487Ter
ENST00000471181.7:c.4522A>T	ENSP00000418960.2:p.Lys1508Ter
ENST00000644379.1:c.846A>T
ENST00000352993.7:c.1033A>T	ENSP00000312236.5:p.Lys345Ter
ENST00000357654.7:c.4459A>T	ENSP00000350283.3:p.Lys1487Ter
ENST00000461221.5:c.*4242A>T	ENSP00000418548.1:n.*4242A>T
ENST00000468300.5:c.1147A>T	ENSP00000417148.1:p.Lys383Ter
ENST00000471181.6:c.4522A>T	ENSP00000418960.2:p.Lys1508Ter
ENST00000478531.5:c.1147A>T	ENSP00000420412.1:p.Lys383Ter
ENST00000484087.5:c.772A>T	ENSP00000419481.1:p.Lys258Ter
ENST00000487825.5:c.775A>T	ENSP00000418212.1:p.Lys259Ter
ENST00000491747.6:c.1147A>T	ENSP00000420705.2:p.Lys383Ter
ENST00000493795.5:c.4318A>T	ENSP00000418775.1:p.Lys1440Ter
ENST00000493919.5:c.1009A>T	ENSP00000418819.1:p.Lys337Ter
ENST00000586385.5:c.5-12562A>T	ENSP00000465818.1:n.5-12562A>T
ENST00000591534.5:c.-43-1992A>T	ENSP00000467329.1:n.-43-1992A>T
ENST00000591849.5:c.-98-26323A>T	ENSP00000465347.1:n.-98-26323A>T
ENST00000621897.1:n.350A>T
NM_007294.3:c.4459A>T , LRG_292t1:c.4459A>T	NP_009225.1:p.Lys1487Ter
NM_007297.3:c.4318A>T	NP_009228.2:p.Lys1440Ter
NM_007298.3:c.1147A>T	NP_009229.2:p.Lys383Ter
NM_007299.3:c.1147A>T	NP_009230.2:p.Lys383Ter
NM_007300.3:c.4522A>T	NP_009231.2:p.Lys1508Ter
NR_027676.1:n.4595A>T
NM_007294.4:c.4459A>T MANE Select	NP_009225.1:p.Lys1487Ter
NM_007297.4:c.4318A>T	NP_009228.2:p.Lys1440Ter
NM_007299.4:c.1147A>T	NP_009230.2:p.Lys383Ter
NM_007300.4:c.4522A>T	NP_009231.2:p.Lys1508Ter
NR_027676.2:n.4636A>T