Canonical Allele Identifier: CA10593204

Gene: BRCA1

Linked Data

• MyVariant Identifiers: chr17:g.41234519T>C (hg19) ; chr17:g.43082502T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43082502T>C , CM000679.2:g.43082502T>C	GRCh38
NC_000017.10:g.41234519T>C , CM000679.1:g.41234519T>C	GRCh37
NC_000017.9:g.38488045T>C	NCBI36
NG_005905.2:g.135482A>G , LRG_292:g.135482A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000461574.2:c.4259A>G	ENSP00000417241.2:p.Gln1420Arg
ENST00000470026.6:c.4259A>G	ENSP00000419274.2:p.Gln1420Arg
ENST00000473961.6:c.4133A>G	ENSP00000420201.2:p.Gln1378Arg
ENST00000476777.6:c.4253A>G	ENSP00000417554.2:p.Gln1418Arg
ENST00000477152.6:c.4181A>G	ENSP00000419988.2:p.Gln1394Arg
ENST00000478531.6:c.947A>G	ENSP00000420412.2:p.Gln316Arg
ENST00000489037.2:c.4181A>G	ENSP00000420781.2:p.Gln1394Arg
ENST00000493919.6:c.809A>G	ENSP00000418819.2:p.Gln270Arg
ENST00000494123.6:c.4259A>G	ENSP00000419103.2:p.Gln1420Arg
ENST00000497488.2:c.3371A>G	ENSP00000418986.2:p.Gln1124Arg
ENST00000618469.2:c.4259A>G	ENSP00000478114.2:p.Gln1420Arg
ENST00000634433.2:c.4136A>G	ENSP00000489431.2:p.Gln1379Arg
ENST00000644379.2:c.4259A>G	ENSP00000496570.2:p.Gln1420Arg
ENST00000644555.2:c.809A>G	ENSP00000494614.2:p.Gln270Arg
ENST00000652672.2:c.4118A>G	ENSP00000498906.2:p.Gln1373Arg
ENST00000484087.6:c.824A>G	ENSP00000419481.2:p.Gln275Arg
ENST00000700182.1:c.869A>G	ENSP00000514849.1:p.Gln290Arg
ENST00000357654.9:c.4259A>G MANE Select	ENSP00000350283.3:p.Gln1420Arg
ENST00000471181.7:c.4259A>G	ENSP00000418960.2:p.Gln1420Arg
ENST00000644379.1:c.580A>G
ENST00000352993.7:c.833A>G	ENSP00000312236.5:p.Gln278Arg
ENST00000357654.7:c.4259A>G	ENSP00000350283.3:p.Gln1420Arg
ENST00000461221.5:c.*4042A>G	ENSP00000418548.1:n.*4042A>G
ENST00000461574.1:c.553A>G
ENST00000468300.5:c.950A>G	ENSP00000417148.1:p.Gln317Arg
ENST00000471181.6:c.4259A>G	ENSP00000418960.2:p.Gln1420Arg
ENST00000478531.5:c.947A>G	ENSP00000420412.1:p.Gln316Arg
ENST00000484087.5:c.572A>G	ENSP00000419481.1:p.Gln191Arg
ENST00000487825.5:c.575A>G	ENSP00000418212.1:p.Gln192Arg
ENST00000491747.6:c.950A>G	ENSP00000420705.2:p.Gln317Arg
ENST00000493795.5:c.4118A>G	ENSP00000418775.1:p.Gln1373Arg
ENST00000493919.5:c.809A>G	ENSP00000418819.1:p.Gln270Arg
ENST00000586385.5:c.5-18551A>G	ENSP00000465818.1:n.5-18551A>G
ENST00000591534.5:c.-43-7981A>G	ENSP00000467329.1:n.-43-7981A>G
ENST00000591849.5:c.-98-32312A>G	ENSP00000465347.1:n.-98-32312A>G
ENST00000621897.1:n.153A>G
NM_007294.3:c.4259A>G , LRG_292t1:c.4259A>G	NP_009225.1:p.Gln1420Arg
NM_007297.3:c.4118A>G	NP_009228.2:p.Gln1373Arg
NM_007298.3:c.950A>G	NP_009229.2:p.Gln317Arg
NM_007299.3:c.950A>G	NP_009230.2:p.Gln317Arg
NM_007300.3:c.4259A>G	NP_009231.2:p.Gln1420Arg
NR_027676.1:n.4395A>G
NM_007294.4:c.4259A>G MANE Select	NP_009225.1:p.Gln1420Arg
NM_007297.4:c.4118A>G	NP_009228.2:p.Gln1373Arg
NM_007299.4:c.950A>G	NP_009230.2:p.Gln317Arg
NM_007300.4:c.4259A>G	NP_009231.2:p.Gln1420Arg
NR_027676.2:n.4436A>G