Canonical Allele Identifier: CA2499224342

Gene: BRCA1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43045760dup , CM000679.2:g.43045760dup	GRCh38
NC_000017.10:g.41197777dup , CM000679.1:g.41197777dup	GRCh37
NC_000017.9:g.38451303dup	NCBI36
NG_005905.2:g.172226dup , LRG_292:g.172226dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461574.2:c.5509dup	ENSP00000417241.2:p.Val1837GlyfsTer?
ENST00000470026.6:c.5512dup	ENSP00000419274.2:p.Val1838GlyfsTer?
ENST00000473961.6:c.5386dup	ENSP00000420201.2:p.Val1796GlyfsTer?
ENST00000476777.6:c.5506dup	ENSP00000417554.2:p.Val1836GlyfsTer?
ENST00000477152.6:c.5434dup	ENSP00000419988.2:p.Val1812GlyfsTer?
ENST00000478531.6:c.2200dup	ENSP00000420412.2:p.Val734GlyfsTer?
ENST00000489037.2:c.5434dup	ENSP00000420781.2:p.Val1812GlyfsTer?
ENST00000493919.6:c.2062dup	ENSP00000418819.2:p.Val688GlyfsTer?
ENST00000494123.6:c.5512dup	ENSP00000419103.2:p.Val1838GlyfsTer?
ENST00000497488.2:c.4624dup	ENSP00000418986.2:p.Val1542GlyfsTer?
ENST00000618469.2:c.5512dup	ENSP00000478114.2:p.Val1838GlyfsTer?
ENST00000634433.2:c.5389dup	ENSP00000489431.2:p.Val1797GlyfsTer?
ENST00000644379.2:c.5578dup	ENSP00000496570.2:p.Val1860GlyfsTer?
ENST00000644555.2:c.2062dup	ENSP00000494614.2:p.Val688GlyfsTer?
ENST00000652672.2:c.5371dup	ENSP00000498906.2:p.Val1791GlyfsTer?
ENST00000484087.6:c.2074dup	ENSP00000419481.2:p.Val692GlyfsTer?
ENST00000700081.1:n.1395dup
ENST00000700082.1:n.876dup
ENST00000357654.9:c.5512dup MANE Select	ENSP00000350283.3:p.Val1838GlyfsTer?
ENST00000471181.7:c.5575dup	ENSP00000418960.2:p.Val1859GlyfsTer?
ENST00000644379.1:c.1899dup
ENST00000352993.7:c.2086dup	ENSP00000312236.5:p.Val696GlyfsTer?
ENST00000357654.7:c.5512dup	ENSP00000350283.3:p.Val1838GlyfsTer?
ENST00000461221.5:c.*5295dup	ENSP00000418548.1:n.*5295dup
ENST00000468300.5:c.*26dup	ENSP00000417148.1:n.*26dup
ENST00000471181.6:c.5575dup	ENSP00000418960.2:p.Val1859GlyfsTer?
ENST00000491747.6:c.2200dup	ENSP00000420705.2:p.Val734GlyfsTer?
ENST00000493795.5:c.5371dup	ENSP00000418775.1:p.Val1791GlyfsTer?
ENST00000586385.5:c.442dup	ENSP00000465818.1:p.Val148GlyfsTer?
ENST00000591534.5:c.985dup	ENSP00000467329.1:p.Val329GlyfsTer?
ENST00000591849.5:c.211dup	ENSP00000465347.1:p.Val71GlyfsTer?
NM_007294.3:c.5512dup , LRG_292t1:c.5512dup	NP_009225.1:p.Val1838GlyfsTer?
NM_007297.3:c.5371dup	NP_009228.2:p.Val1791GlyfsTer?
NM_007298.3:c.2200dup	NP_009229.2:p.Val734GlyfsTer?
NM_007299.3:c.*26dup	NP_009230.2:n.*26dup
NM_007300.3:c.5575dup	NP_009231.2:p.Val1859GlyfsTer?
NR_027676.1:n.5648dup
NM_007294.4:c.5512dup MANE Select	NP_009225.1:p.Val1838GlyfsTer?
NM_007297.4:c.5371dup	NP_009228.2:p.Val1791GlyfsTer?
NM_007299.4:c.*26dup	NP_009230.2:n.*26dup
NM_007300.4:c.5575dup	NP_009231.2:p.Val1859GlyfsTer?
NR_027676.2:n.5689dup