Canonical Allele Identifier: CA2260777166
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43080398T= , CM000679.2:g.43080398T= GRCh38
NC_000017.10:g.41232415T= , CM000679.1:g.41232415T= GRCh37
NC_000017.9:g.38485941T= NCBI36
NG_005905.2:g.137586A= , LRG_292:g.137586A=

Transcript Alleles

HGVS Amino-acid change
ENST00000461574.2:c.4357+2006A= ENSP00000417241.2:n.4357+2006A=
ENST00000470026.6:c.4357+2006A= ENSP00000419274.2:n.4357+2006A=
ENST00000473961.6:c.4231+2006A= ENSP00000420201.2:n.4231+2006A=
ENST00000476777.6:c.4351+2006A= ENSP00000417554.2:n.4351+2006A=
ENST00000477152.6:c.4279+2006A= ENSP00000419988.2:n.4279+2006A=
ENST00000478531.6:c.1045+2006A= ENSP00000420412.2:n.1045+2006A=
ENST00000489037.2:c.4279+2006A= ENSP00000420781.2:n.4279+2006A=
ENST00000493919.6:c.907+2006A= ENSP00000418819.2:n.907+2006A=
ENST00000494123.6:c.4357+2006A= ENSP00000419103.2:n.4357+2006A=
ENST00000497488.2:c.3469+2006A= ENSP00000418986.2:n.3469+2006A=
ENST00000618469.2:c.4357+2006A= ENSP00000478114.2:n.4357+2006A=
ENST00000634433.2:c.4234+2006A= ENSP00000489431.2:n.4234+2006A=
ENST00000644379.2:c.4358-999A= ENSP00000496570.2:n.4358-999A=
ENST00000644555.2:c.907+2006A= ENSP00000494614.2:n.907+2006A=
ENST00000652672.2:c.4216+2006A= ENSP00000498906.2:n.4216+2006A=
ENST00000484087.6:c.922+2006A= ENSP00000419481.2:n.922+2006A=
ENST00000700182.1:c.967+2006A= ENSP00000514849.1:n.967+2006A=
ENST00000357654.9:c.4357+2006A= MANE Select ENSP00000350283.3:n.4357+2006A=
ENST00000471181.7:c.4358-999A= ENSP00000418960.2:n.4358-999A=
ENST00000644379.1:c.679-999A=
ENST00000352993.7:c.931+2006A= ENSP00000312236.5:n.931+2006A=
ENST00000357654.7:c.4357+2006A= ENSP00000350283.3:n.4357+2006A=
ENST00000461221.5:c.*4140+2006A= ENSP00000418548.1:n.*4140+2006A=
ENST00000461574.1:c.651+2006A=
ENST00000468300.5:c.1048+2006A= ENSP00000417148.1:n.1048+2006A=
ENST00000471181.6:c.4358-999A= ENSP00000418960.2:n.4358-999A=
ENST00000478531.5:c.1045+2006A= ENSP00000420412.1:n.1045+2006A=
ENST00000484087.5:c.670+2006A= ENSP00000419481.1:n.670+2006A=
ENST00000487825.5:c.673+2006A= ENSP00000418212.1:n.673+2006A=
ENST00000491747.6:c.1048+2006A= ENSP00000420705.2:n.1048+2006A=
ENST00000493795.5:c.4216+2006A= ENSP00000418775.1:n.4216+2006A=
ENST00000493919.5:c.907+2006A= ENSP00000418819.1:n.907+2006A=
ENST00000586385.5:c.5-16447A= ENSP00000465818.1:n.5-16447A=
ENST00000591534.5:c.-43-5877A= ENSP00000467329.1:n.-43-5877A=
ENST00000591849.5:c.-98-30208A= ENSP00000465347.1:n.-98-30208A=
ENST00000621897.1:n.251+2006A=
NM_007294.3:c.4357+2006A= , LRG_292t1:c.4357+2006A= NP_009225.1:n.4357+2006A=
NM_007297.3:c.4216+2006A= NP_009228.2:n.4216+2006A=
NM_007298.3:c.1048+2006A= NP_009229.2:n.1048+2006A=
NM_007299.3:c.1048+2006A= NP_009230.2:n.1048+2006A=
NM_007300.3:c.4358-999A= NP_009231.2:n.4358-999A=
NR_027676.1:n.4493+2006A=
NM_007294.4:c.4357+2006A= MANE Select NP_009225.1:n.4357+2006A=
NM_007297.4:c.4216+2006A= NP_009228.2:n.4216+2006A=
NM_007299.4:c.1048+2006A= NP_009230.2:n.1048+2006A=
NM_007300.4:c.4358-999A= NP_009231.2:n.4358-999A=
NR_027676.2:n.4534+2006A=