Canonical Allele Identifier: CA2260785351
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43094871A= , CM000679.2:g.43094871A= GRCh38
NC_000017.10:g.41246888A= , CM000679.1:g.41246888A= GRCh37
NC_000017.9:g.38500414A= NCBI36
NG_005905.2:g.123113T= , LRG_292:g.123113T=

Transcript Alleles

HGVS Amino-acid change
ENST00000354071.8:n.735-11T=
ENST00000461574.2:c.671-11T= ENSP00000417241.2:n.671-11T=
ENST00000470026.6:c.671-11T= ENSP00000419274.2:n.671-11T=
ENST00000473961.6:c.545-11T= ENSP00000420201.2:n.545-11T=
ENST00000476777.6:c.668-11T= ENSP00000417554.2:n.668-11T=
ENST00000477152.6:c.593-11T= ENSP00000419988.2:n.593-11T=
ENST00000478531.6:c.668-11T= ENSP00000420412.2:n.668-11T=
ENST00000489037.2:c.593-11T= ENSP00000420781.2:n.593-11T=
ENST00000493919.6:c.530-11T= ENSP00000418819.2:n.530-11T=
ENST00000494123.6:c.671-11T= ENSP00000419103.2:n.671-11T=
ENST00000497488.2:c.-218-11T= ENSP00000418986.2:n.-218-11T=
ENST00000618469.2:c.671-11T= ENSP00000478114.2:n.671-11T=
ENST00000634433.2:c.548-11T= ENSP00000489431.2:n.548-11T=
ENST00000644379.2:c.671-11T= ENSP00000496570.2:n.671-11T=
ENST00000644555.2:c.530-11T= ENSP00000494614.2:n.530-11T=
ENST00000652672.2:c.530-11T= ENSP00000498906.2:n.530-11T=
ENST00000484087.6:c.548-11T= ENSP00000419481.2:n.548-11T=
ENST00000700182.1:c.590-11T= ENSP00000514849.1:n.590-11T=
ENST00000700183.1:c.*679-11T= ENSP00000514850.1:n.*679-11T=
ENST00000357654.9:c.671-11T= MANE Select ENSP00000350283.3:n.671-11T=
ENST00000471181.7:c.671-11T= ENSP00000418960.2:n.671-11T=
ENST00000642945.1:c.*545-11T= ENSP00000495897.1:n.*545-11T=
ENST00000652672.1:c.530-11T= ENSP00000498906.1:n.530-11T=
ENST00000352993.7:c.670+975T= ENSP00000312236.5:n.670+975T=
ENST00000354071.7:c.671-11T= ENSP00000326002.7:n.671-11T=
ENST00000357654.7:c.671-11T= ENSP00000350283.3:n.671-11T=
ENST00000412061.3:c.22-11T=
ENST00000461221.5:c.*454-11T= ENSP00000418548.1:n.*454-11T=
ENST00000468300.5:c.671-11T= ENSP00000417148.1:n.671-11T=
ENST00000470026.5:c.671-11T= ENSP00000419274.1:n.671-11T=
ENST00000471181.6:c.671-11T= ENSP00000418960.2:n.671-11T=
ENST00000473961.5:c.268-11T=
ENST00000477152.5:c.593-11T= ENSP00000419988.1:n.593-11T=
ENST00000478531.5:c.668-11T= ENSP00000420412.1:n.668-11T=
ENST00000484087.5:c.293-11T= ENSP00000419481.1:n.293-11T=
ENST00000487825.5:c.296-11T= ENSP00000418212.1:n.296-11T=
ENST00000491747.6:c.671-11T= ENSP00000420705.2:n.671-11T=
ENST00000492859.5:c.*607-11T= ENSP00000420253.1:n.*607-11T=
ENST00000493795.5:c.530-11T= ENSP00000418775.1:n.530-11T=
ENST00000493919.5:c.530-11T= ENSP00000418819.1:n.530-11T=
ENST00000494123.5:c.671-11T= ENSP00000419103.1:n.671-11T=
ENST00000497488.1:c.-218-11T= ENSP00000418986.1:n.-218-11T=
ENST00000586385.5:c.4+30311T= ENSP00000465818.1:n.4+30311T=
ENST00000591534.5:c.-43-20350T= ENSP00000467329.1:n.-43-20350T=
ENST00000591849.5:c.-99+30400T= ENSP00000465347.1:n.-99+30400T=
ENST00000634433.1:c.548-11T= ENSP00000489431.1:n.548-11T=
NM_007294.3:c.671-11T= , LRG_292t1:c.671-11T= NP_009225.1:n.671-11T=
NM_007297.3:c.530-11T= NP_009228.2:n.530-11T=
NM_007298.3:c.671-11T= NP_009229.2:n.671-11T=
NM_007299.3:c.671-11T= NP_009230.2:n.671-11T=
NM_007300.3:c.671-11T= NP_009231.2:n.671-11T=
NR_027676.1:n.807-11T=
NM_007294.4:c.671-11T= MANE Select NP_009225.1:n.671-11T=
NM_007297.4:c.530-11T= NP_009228.2:n.530-11T=
NM_007299.4:c.671-11T= NP_009230.2:n.671-11T=
NM_007300.4:c.671-11T= NP_009231.2:n.671-11T=
NR_027676.2:n.848-11T=