Canonical Allele Identifier: CA10593494

Gene: BRCA1

Linked Data - Expert Curation

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43091012C>T , CM000679.2:g.43091012C>T	GRCh38
NC_000017.10:g.41243029C>T , CM000679.1:g.41243029C>T	GRCh37
NC_000017.9:g.38496555C>T	NCBI36
NG_005905.2:g.126972G>A , LRG_292:g.126972G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461574.2:c.4117G>A	ENSP00000417241.2:p.Glu1373Lys
ENST00000470026.6:c.4117G>A	ENSP00000419274.2:p.Glu1373Lys
ENST00000473961.6:c.3991G>A	ENSP00000420201.2:p.Glu1331Lys
ENST00000476777.6:c.4114G>A	ENSP00000417554.2:p.Glu1372Lys
ENST00000477152.6:c.4039G>A	ENSP00000419988.2:p.Glu1347Lys
ENST00000478531.6:c.805G>A	ENSP00000420412.2:p.Glu269Lys
ENST00000489037.2:c.4039G>A	ENSP00000420781.2:p.Glu1347Lys
ENST00000493919.6:c.667G>A	ENSP00000418819.2:p.Glu223Lys
ENST00000494123.6:c.4117G>A	ENSP00000419103.2:p.Glu1373Lys
ENST00000497488.2:c.3229G>A	ENSP00000418986.2:p.Glu1077Lys
ENST00000618469.2:c.4117G>A	ENSP00000478114.2:p.Glu1373Lys
ENST00000634433.2:c.3994G>A	ENSP00000489431.2:p.Glu1332Lys
ENST00000644379.2:c.4117G>A	ENSP00000496570.2:p.Glu1373Lys
ENST00000644555.2:c.667G>A	ENSP00000494614.2:p.Glu223Lys
ENST00000652672.2:c.3976G>A	ENSP00000498906.2:p.Glu1326Lys
ENST00000484087.6:c.685G>A	ENSP00000419481.2:p.Glu229Lys
ENST00000700182.1:c.727G>A	ENSP00000514849.1:p.Glu243Lys
ENST00000357654.9:c.4117G>A MANE Select	ENSP00000350283.3:p.Glu1373Lys
ENST00000471181.7:c.4117G>A	ENSP00000418960.2:p.Glu1373Lys
ENST00000644379.1:c.438G>A
ENST00000352993.7:c.691G>A	ENSP00000312236.5:p.Glu231Lys
ENST00000357654.7:c.4117G>A	ENSP00000350283.3:p.Glu1373Lys
ENST00000461221.5:c.*3900G>A	ENSP00000418548.1:n.*3900G>A
ENST00000461574.1:c.411G>A
ENST00000468300.5:c.808G>A	ENSP00000417148.1:p.Glu270Lys
ENST00000471181.6:c.4117G>A	ENSP00000418960.2:p.Glu1373Lys
ENST00000478531.5:c.805G>A	ENSP00000420412.1:p.Glu269Lys
ENST00000484087.5:c.430G>A	ENSP00000419481.1:p.Glu144Lys
ENST00000487825.5:c.433G>A	ENSP00000418212.1:p.Glu145Lys
ENST00000491747.6:c.808G>A	ENSP00000420705.2:p.Glu270Lys
ENST00000493795.5:c.3976G>A	ENSP00000418775.1:p.Glu1326Lys
ENST00000493919.5:c.667G>A	ENSP00000418819.1:p.Glu223Lys
ENST00000586385.5:c.5-27061G>A	ENSP00000465818.1:n.5-27061G>A
ENST00000591534.5:c.-43-16491G>A	ENSP00000467329.1:n.-43-16491G>A
ENST00000591849.5:c.-99+34259G>A	ENSP00000465347.1:n.-99+34259G>A
NM_007294.3:c.4117G>A , LRG_292t1:c.4117G>A	NP_009225.1:p.Glu1373Lys
NM_007297.3:c.3976G>A	NP_009228.2:p.Glu1326Lys
NM_007298.3:c.808G>A	NP_009229.2:p.Glu270Lys
NM_007299.3:c.808G>A	NP_009230.2:p.Glu270Lys
NM_007300.3:c.4117G>A	NP_009231.2:p.Glu1373Lys
NR_027676.1:n.4253G>A
NM_007294.4:c.4117G>A MANE Select	NP_009225.1:p.Glu1373Lys
NM_007297.4:c.3976G>A	NP_009228.2:p.Glu1326Lys
NM_007299.4:c.808G>A	NP_009230.2:p.Glu270Lys
NM_007300.4:c.4117G>A	NP_009231.2:p.Glu1373Lys
NR_027676.2:n.4294G>A