Canonical Allele Identifier: CA2260777952
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43082407T= , CM000679.2:g.43082407T= GRCh38
NC_000017.10:g.41234424T= , CM000679.1:g.41234424T= GRCh37
NC_000017.9:g.38487950T= NCBI36
NG_005905.2:g.135577A= , LRG_292:g.135577A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000461574.2:c.4354A= ENSP00000417241.2:p.Lys1452=
ENST00000470026.6:c.4354A= ENSP00000419274.2:p.Lys1452=
ENST00000473961.6:c.4228A= ENSP00000420201.2:p.Lys1410=
ENST00000476777.6:c.4348A= ENSP00000417554.2:p.Lys1450=
ENST00000477152.6:c.4276A= ENSP00000419988.2:p.Lys1426=
ENST00000478531.6:c.1042A= ENSP00000420412.2:p.Lys348=
ENST00000489037.2:c.4276A= ENSP00000420781.2:p.Lys1426=
ENST00000493919.6:c.904A= ENSP00000418819.2:p.Lys302=
ENST00000494123.6:c.4354A= ENSP00000419103.2:p.Lys1452=
ENST00000497488.2:c.3466A= ENSP00000418986.2:p.Lys1156=
ENST00000618469.2:c.4354A= ENSP00000478114.2:p.Lys1452=
ENST00000634433.2:c.4231A= ENSP00000489431.2:p.Lys1411=
ENST00000644379.2:c.4354A= ENSP00000496570.2:p.Lys1452=
ENST00000644555.2:c.904A= ENSP00000494614.2:p.Lys302=
ENST00000652672.2:c.4213A= ENSP00000498906.2:p.Lys1405=
ENST00000484087.6:c.919A= ENSP00000419481.2:p.Lys307=
ENST00000700182.1:c.964A= ENSP00000514849.1:p.Lys322=
ENST00000357654.9:c.4354A= MANE Select ENSP00000350283.3:p.Lys1452=
ENST00000471181.7:c.4354A= ENSP00000418960.2:p.Lys1452=
ENST00000644379.1:c.675A=
ENST00000352993.7:c.928A= ENSP00000312236.5:p.Lys310=
ENST00000357654.7:c.4354A= ENSP00000350283.3:p.Lys1452=
ENST00000461221.5:c.*4137A= ENSP00000418548.1:n.*4137A=
ENST00000461574.1:c.648A=
ENST00000468300.5:c.1045A= ENSP00000417148.1:p.Lys349=
ENST00000471181.6:c.4354A= ENSP00000418960.2:p.Lys1452=
ENST00000478531.5:c.1042A= ENSP00000420412.1:p.Lys348=
ENST00000484087.5:c.667A= ENSP00000419481.1:p.Lys223=
ENST00000487825.5:c.670A= ENSP00000418212.1:p.Lys224=
ENST00000491747.6:c.1045A= ENSP00000420705.2:p.Lys349=
ENST00000493795.5:c.4213A= ENSP00000418775.1:p.Lys1405=
ENST00000493919.5:c.904A= ENSP00000418819.1:p.Lys302=
ENST00000586385.5:c.5-18456A= ENSP00000465818.1:n.5-18456A=
ENST00000591534.5:c.-43-7886A= ENSP00000467329.1:n.-43-7886A=
ENST00000591849.5:c.-98-32217A= ENSP00000465347.1:n.-98-32217A=
ENST00000621897.1:n.248A=
NM_007294.3:c.4354A= , LRG_292t1:c.4354A= NP_009225.1:p.Lys1452=
NM_007297.3:c.4213A= NP_009228.2:p.Lys1405=
NM_007298.3:c.1045A= NP_009229.2:p.Lys349=
NM_007299.3:c.1045A= NP_009230.2:p.Lys349=
NM_007300.3:c.4354A= NP_009231.2:p.Lys1452=
NR_027676.1:n.4490A=
NM_007294.4:c.4354A= MANE Select NP_009225.1:p.Lys1452=
NM_007297.4:c.4213A= NP_009228.2:p.Lys1405=
NM_007299.4:c.1045A= NP_009230.2:p.Lys349=
NM_007300.4:c.4354A= NP_009231.2:p.Lys1452=
NR_027676.2:n.4531A=