Canonical Allele Identifier: CA2260777938
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43082393A= , CM000679.2:g.43082393A= GRCh38
NC_000017.10:g.41234410A= , CM000679.1:g.41234410A= GRCh37
NC_000017.9:g.38487936A= NCBI36
NG_005905.2:g.135591T= , LRG_292:g.135591T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000461574.2:c.4357+11T= ENSP00000417241.2:n.4357+11T=
ENST00000470026.6:c.4357+11T= ENSP00000419274.2:n.4357+11T=
ENST00000473961.6:c.4231+11T= ENSP00000420201.2:n.4231+11T=
ENST00000476777.6:c.4351+11T= ENSP00000417554.2:n.4351+11T=
ENST00000477152.6:c.4279+11T= ENSP00000419988.2:n.4279+11T=
ENST00000478531.6:c.1045+11T= ENSP00000420412.2:n.1045+11T=
ENST00000489037.2:c.4279+11T= ENSP00000420781.2:n.4279+11T=
ENST00000493919.6:c.907+11T= ENSP00000418819.2:n.907+11T=
ENST00000494123.6:c.4357+11T= ENSP00000419103.2:n.4357+11T=
ENST00000497488.2:c.3469+11T= ENSP00000418986.2:n.3469+11T=
ENST00000618469.2:c.4357+11T= ENSP00000478114.2:n.4357+11T=
ENST00000634433.2:c.4234+11T= ENSP00000489431.2:n.4234+11T=
ENST00000644379.2:c.4357+11T= ENSP00000496570.2:n.4357+11T=
ENST00000644555.2:c.907+11T= ENSP00000494614.2:n.907+11T=
ENST00000652672.2:c.4216+11T= ENSP00000498906.2:n.4216+11T=
ENST00000484087.6:c.922+11T= ENSP00000419481.2:n.922+11T=
ENST00000700182.1:c.967+11T= ENSP00000514849.1:n.967+11T=
ENST00000357654.9:c.4357+11T= MANE Select ENSP00000350283.3:n.4357+11T=
ENST00000471181.7:c.4357+11T= ENSP00000418960.2:n.4357+11T=
ENST00000644379.1:c.678+11T=
ENST00000352993.7:c.931+11T= ENSP00000312236.5:n.931+11T=
ENST00000357654.7:c.4357+11T= ENSP00000350283.3:n.4357+11T=
ENST00000461221.5:c.*4140+11T= ENSP00000418548.1:n.*4140+11T=
ENST00000461574.1:c.651+11T=
ENST00000468300.5:c.1048+11T= ENSP00000417148.1:n.1048+11T=
ENST00000471181.6:c.4357+11T= ENSP00000418960.2:n.4357+11T=
ENST00000478531.5:c.1045+11T= ENSP00000420412.1:n.1045+11T=
ENST00000484087.5:c.670+11T= ENSP00000419481.1:n.670+11T=
ENST00000487825.5:c.673+11T= ENSP00000418212.1:n.673+11T=
ENST00000491747.6:c.1048+11T= ENSP00000420705.2:n.1048+11T=
ENST00000493795.5:c.4216+11T= ENSP00000418775.1:n.4216+11T=
ENST00000493919.5:c.907+11T= ENSP00000418819.1:n.907+11T=
ENST00000586385.5:c.5-18442T= ENSP00000465818.1:n.5-18442T=
ENST00000591534.5:c.-43-7872T= ENSP00000467329.1:n.-43-7872T=
ENST00000591849.5:c.-98-32203T= ENSP00000465347.1:n.-98-32203T=
ENST00000621897.1:n.251+11T=
NM_007294.3:c.4357+11T= , LRG_292t1:c.4357+11T= NP_009225.1:n.4357+11T=
NM_007297.3:c.4216+11T= NP_009228.2:n.4216+11T=
NM_007298.3:c.1048+11T= NP_009229.2:n.1048+11T=
NM_007299.3:c.1048+11T= NP_009230.2:n.1048+11T=
NM_007300.3:c.4357+11T= NP_009231.2:n.4357+11T=
NR_027676.1:n.4493+11T=
NM_007294.4:c.4357+11T= MANE Select NP_009225.1:n.4357+11T=
NM_007297.4:c.4216+11T= NP_009228.2:n.4216+11T=
NM_007299.4:c.1048+11T= NP_009230.2:n.1048+11T=
NM_007300.4:c.4357+11T= NP_009231.2:n.4357+11T=
NR_027676.2:n.4534+11T=