Canonical Allele Identifier: CA500148380

Gene: BRCA1

Linked Data

• dbSNP Id: rs2154151429
• MyVariant Identifiers: chr17:g.41234485G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43082468G>A , CM000679.2:g.43082468G>A	GRCh38
NC_000017.10:g.41234485G>A , CM000679.1:g.41234485G>A	GRCh37
NC_000017.9:g.38488011G>A	NCBI36
NG_005905.2:g.135516C>T , LRG_292:g.135516C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000461574.2:c.4293C>T	ENSP00000417241.2:p.Ser1431=
ENST00000470026.6:c.4293C>T	ENSP00000419274.2:p.Ser1431=
ENST00000473961.6:c.4167C>T	ENSP00000420201.2:p.Ser1389=
ENST00000476777.6:c.4287C>T	ENSP00000417554.2:p.Ser1429=
ENST00000477152.6:c.4215C>T	ENSP00000419988.2:p.Ser1405=
ENST00000478531.6:c.981C>T	ENSP00000420412.2:p.Ser327=
ENST00000489037.2:c.4215C>T	ENSP00000420781.2:p.Ser1405=
ENST00000493919.6:c.843C>T	ENSP00000418819.2:p.Ser281=
ENST00000494123.6:c.4293C>T	ENSP00000419103.2:p.Ser1431=
ENST00000497488.2:c.3405C>T	ENSP00000418986.2:p.Ser1135=
ENST00000618469.2:c.4293C>T	ENSP00000478114.2:p.Ser1431=
ENST00000634433.2:c.4170C>T	ENSP00000489431.2:p.Ser1390=
ENST00000644379.2:c.4293C>T	ENSP00000496570.2:p.Ser1431=
ENST00000644555.2:c.843C>T	ENSP00000494614.2:p.Ser281=
ENST00000652672.2:c.4152C>T	ENSP00000498906.2:p.Ser1384=
ENST00000484087.6:c.858C>T	ENSP00000419481.2:p.Ser286=
ENST00000700182.1:c.903C>T	ENSP00000514849.1:p.Ser301=
ENST00000357654.9:c.4293C>T MANE Select	ENSP00000350283.3:p.Ser1431=
ENST00000471181.7:c.4293C>T	ENSP00000418960.2:p.Ser1431=
ENST00000644379.1:c.614C>T
ENST00000352993.7:c.867C>T	ENSP00000312236.5:p.Ser289=
ENST00000357654.7:c.4293C>T	ENSP00000350283.3:p.Ser1431=
ENST00000461221.5:c.*4076C>T	ENSP00000418548.1:n.*4076C>T
ENST00000461574.1:c.587C>T
ENST00000468300.5:c.984C>T	ENSP00000417148.1:p.Ser328=
ENST00000471181.6:c.4293C>T	ENSP00000418960.2:p.Ser1431=
ENST00000478531.5:c.981C>T	ENSP00000420412.1:p.Ser327=
ENST00000484087.5:c.606C>T	ENSP00000419481.1:p.Ser202=
ENST00000487825.5:c.609C>T	ENSP00000418212.1:p.Ser203=
ENST00000491747.6:c.984C>T	ENSP00000420705.2:p.Ser328=
ENST00000493795.5:c.4152C>T	ENSP00000418775.1:p.Ser1384=
ENST00000493919.5:c.843C>T	ENSP00000418819.1:p.Ser281=
ENST00000586385.5:c.5-18517C>T	ENSP00000465818.1:n.5-18517C>T
ENST00000591534.5:c.-43-7947C>T	ENSP00000467329.1:n.-43-7947C>T
ENST00000591849.5:c.-98-32278C>T	ENSP00000465347.1:n.-98-32278C>T
ENST00000621897.1:n.187C>T
NM_007294.3:c.4293C>T , LRG_292t1:c.4293C>T	NP_009225.1:p.Ser1431=
NM_007297.3:c.4152C>T	NP_009228.2:p.Ser1384=
NM_007298.3:c.984C>T	NP_009229.2:p.Ser328=
NM_007299.3:c.984C>T	NP_009230.2:p.Ser328=
NM_007300.3:c.4293C>T	NP_009231.2:p.Ser1431=
NR_027676.1:n.4429C>T
NM_007294.4:c.4293C>T MANE Select	NP_009225.1:p.Ser1431=
NM_007297.4:c.4152C>T	NP_009228.2:p.Ser1384=
NM_007299.4:c.984C>T	NP_009230.2:p.Ser328=
NM_007300.4:c.4293C>T	NP_009231.2:p.Ser1431=
NR_027676.2:n.4470C>T