Canonical Allele Identifier: CA10593314

Gene: BRCA1

Linked Data

• MyVariant Identifiers: chr17:g.41234575T>G (hg19) ; chr17:g.43082558T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43082558T>G , CM000679.2:g.43082558T>G	GRCh38
NC_000017.10:g.41234575T>G , CM000679.1:g.41234575T>G	GRCh37
NC_000017.9:g.38488101T>G	NCBI36
NG_005905.2:g.135426A>C , LRG_292:g.135426A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461574.2:c.4203A>C	ENSP00000417241.2:p.Gln1401His
ENST00000470026.6:c.4203A>C	ENSP00000419274.2:p.Gln1401His
ENST00000473961.6:c.4077A>C	ENSP00000420201.2:p.Gln1359His
ENST00000476777.6:c.4197A>C	ENSP00000417554.2:p.Gln1399His
ENST00000477152.6:c.4125A>C	ENSP00000419988.2:p.Gln1375His
ENST00000478531.6:c.891A>C	ENSP00000420412.2:p.Gln297His
ENST00000489037.2:c.4125A>C	ENSP00000420781.2:p.Gln1375His
ENST00000493919.6:c.753A>C	ENSP00000418819.2:p.Gln251His
ENST00000494123.6:c.4203A>C	ENSP00000419103.2:p.Gln1401His
ENST00000497488.2:c.3315A>C	ENSP00000418986.2:p.Gln1105His
ENST00000618469.2:c.4203A>C	ENSP00000478114.2:p.Gln1401His
ENST00000634433.2:c.4080A>C	ENSP00000489431.2:p.Gln1360His
ENST00000644379.2:c.4203A>C	ENSP00000496570.2:p.Gln1401His
ENST00000644555.2:c.753A>C	ENSP00000494614.2:p.Gln251His
ENST00000652672.2:c.4062A>C	ENSP00000498906.2:p.Gln1354His
ENST00000484087.6:c.768A>C	ENSP00000419481.2:p.Gln256His
ENST00000700182.1:c.813A>C	ENSP00000514849.1:p.Gln271His
ENST00000357654.9:c.4203A>C MANE Select	ENSP00000350283.3:p.Gln1401His
ENST00000471181.7:c.4203A>C	ENSP00000418960.2:p.Gln1401His
ENST00000644379.1:c.524A>C
ENST00000352993.7:c.777A>C	ENSP00000312236.5:p.Gln259His
ENST00000357654.7:c.4203A>C	ENSP00000350283.3:p.Gln1401His
ENST00000461221.5:c.*3986A>C	ENSP00000418548.1:n.*3986A>C
ENST00000461574.1:c.497A>C
ENST00000468300.5:c.894A>C	ENSP00000417148.1:p.Gln298His
ENST00000471181.6:c.4203A>C	ENSP00000418960.2:p.Gln1401His
ENST00000478531.5:c.891A>C	ENSP00000420412.1:p.Gln297His
ENST00000484087.5:c.516A>C	ENSP00000419481.1:p.Gln172His
ENST00000487825.5:c.519A>C	ENSP00000418212.1:p.Gln173His
ENST00000491747.6:c.894A>C	ENSP00000420705.2:p.Gln298His
ENST00000493795.5:c.4062A>C	ENSP00000418775.1:p.Gln1354His
ENST00000493919.5:c.753A>C	ENSP00000418819.1:p.Gln251His
ENST00000586385.5:c.5-18607A>C	ENSP00000465818.1:n.5-18607A>C
ENST00000591534.5:c.-43-8037A>C	ENSP00000467329.1:n.-43-8037A>C
ENST00000591849.5:c.-98-32368A>C	ENSP00000465347.1:n.-98-32368A>C
ENST00000621897.1:n.97A>C
NM_007294.3:c.4203A>C , LRG_292t1:c.4203A>C	NP_009225.1:p.Gln1401His
NM_007297.3:c.4062A>C	NP_009228.2:p.Gln1354His
NM_007298.3:c.894A>C	NP_009229.2:p.Gln298His
NM_007299.3:c.894A>C	NP_009230.2:p.Gln298His
NM_007300.3:c.4203A>C	NP_009231.2:p.Gln1401His
NR_027676.1:n.4339A>C
NM_007294.4:c.4203A>C MANE Select	NP_009225.1:p.Gln1401His
NM_007297.4:c.4062A>C	NP_009228.2:p.Gln1354His
NM_007299.4:c.894A>C	NP_009230.2:p.Gln298His
NM_007300.4:c.4203A>C	NP_009231.2:p.Gln1401His
NR_027676.2:n.4380A>C