Canonical Allele Identifier: CA10592568

Gene: BRCA1

Linked Data

• gnomAD v4: 17-43076489-T-C
• MyVariant Identifiers: chr17:g.41228506T>C (hg19) ; chr17:g.43076489T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43076489T>C , CM000679.2:g.43076489T>C	GRCh38
NC_000017.10:g.41228506T>C , CM000679.1:g.41228506T>C	GRCh37
NC_000017.9:g.38482032T>C	NCBI36
NG_005905.2:g.141495A>G , LRG_292:g.141495A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461574.2:c.4480A>G	ENSP00000417241.2:p.Arg1494Gly
ENST00000470026.6:c.4483A>G	ENSP00000419274.2:p.Arg1495Gly
ENST00000473961.6:c.4357A>G	ENSP00000420201.2:p.Arg1453Gly
ENST00000476777.6:c.4477A>G	ENSP00000417554.2:p.Arg1493Gly
ENST00000477152.6:c.4405A>G	ENSP00000419988.2:p.Arg1469Gly
ENST00000478531.6:c.1171A>G	ENSP00000420412.2:p.Arg391Gly
ENST00000489037.2:c.4405A>G	ENSP00000420781.2:p.Arg1469Gly
ENST00000493919.6:c.1033A>G	ENSP00000418819.2:p.Arg345Gly
ENST00000494123.6:c.4483A>G	ENSP00000419103.2:p.Arg1495Gly
ENST00000497488.2:c.3595A>G	ENSP00000418986.2:p.Arg1199Gly
ENST00000618469.2:c.4483A>G	ENSP00000478114.2:p.Arg1495Gly
ENST00000634433.2:c.4360A>G	ENSP00000489431.2:p.Arg1454Gly
ENST00000644379.2:c.4549A>G	ENSP00000496570.2:p.Arg1517Gly
ENST00000644555.2:c.1033A>G	ENSP00000494614.2:p.Arg345Gly
ENST00000652672.2:c.4342A>G	ENSP00000498906.2:p.Arg1448Gly
ENST00000484087.6:c.1045A>G	ENSP00000419481.2:p.Arg349Gly
ENST00000700182.1:c.1090A>G	ENSP00000514849.1:p.Arg364Gly
ENST00000357654.9:c.4483A>G MANE Select	ENSP00000350283.3:p.Arg1495Gly
ENST00000471181.7:c.4546A>G	ENSP00000418960.2:p.Arg1516Gly
ENST00000644379.1:c.870A>G
ENST00000352993.7:c.1057A>G	ENSP00000312236.5:p.Arg353Gly
ENST00000357654.7:c.4483A>G	ENSP00000350283.3:p.Arg1495Gly
ENST00000461221.5:c.*4266A>G	ENSP00000418548.1:n.*4266A>G
ENST00000468300.5:c.1171A>G	ENSP00000417148.1:p.Arg391Gly
ENST00000471181.6:c.4546A>G	ENSP00000418960.2:p.Arg1516Gly
ENST00000478531.5:c.1171A>G	ENSP00000420412.1:p.Arg391Gly
ENST00000484087.5:c.796A>G	ENSP00000419481.1:p.Arg266Gly
ENST00000487825.5:c.799A>G
ENST00000491747.6:c.1171A>G	ENSP00000420705.2:p.Arg391Gly
ENST00000493795.5:c.4342A>G	ENSP00000418775.1:p.Arg1448Gly
ENST00000493919.5:c.1033A>G	ENSP00000418819.1:p.Arg345Gly
ENST00000586385.5:c.5-12538A>G	ENSP00000465818.1:n.5-12538A>G
ENST00000591534.5:c.-43-1968A>G	ENSP00000467329.1:n.-43-1968A>G
ENST00000591849.5:c.-98-26299A>G	ENSP00000465347.1:n.-98-26299A>G
ENST00000621897.1:n.374A>G
NM_007294.3:c.4483A>G , LRG_292t1:c.4483A>G	NP_009225.1:p.Arg1495Gly
NM_007297.3:c.4342A>G	NP_009228.2:p.Arg1448Gly
NM_007298.3:c.1171A>G	NP_009229.2:p.Arg391Gly
NM_007299.3:c.1171A>G	NP_009230.2:p.Arg391Gly
NM_007300.3:c.4546A>G	NP_009231.2:p.Arg1516Gly
NR_027676.1:n.4619A>G
NM_007294.4:c.4483A>G MANE Select	NP_009225.1:p.Arg1495Gly
NM_007297.4:c.4342A>G	NP_009228.2:p.Arg1448Gly
NM_007299.4:c.1171A>G	NP_009230.2:p.Arg391Gly
NM_007300.4:c.4546A>G	NP_009231.2:p.Arg1516Gly
NR_027676.2:n.4660A>G