Canonical Allele Identifier: CA2260777866
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43082231_43082233delinsCCT , CM000679.2:g.43082231_43082233delinsCCT GRCh38
NC_000017.10:g.41234248_41234250delinsCCT , CM000679.1:g.41234248_41234250delinsCCT GRCh37
NC_000017.9:g.38487774_38487776delinsCCT NCBI36
NG_005905.2:g.135751_135753delinsAGG , LRG_292:g.135751_135753delinsAGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000461574.2:c.4357+171_4357+173delinsAGG ENSP00000417241.2:n.4357+171_4357+173delinsAGG
ENST00000470026.6:c.4357+171_4357+173delinsAGG ENSP00000419274.2:n.4357+171_4357+173delinsAGG
ENST00000473961.6:c.4231+171_4231+173delinsAGG ENSP00000420201.2:n.4231+171_4231+173delinsAGG
ENST00000476777.6:c.4351+171_4351+173delinsAGG ENSP00000417554.2:n.4351+171_4351+173delinsAGG
ENST00000477152.6:c.4279+171_4279+173delinsAGG ENSP00000419988.2:n.4279+171_4279+173delinsAGG
ENST00000478531.6:c.1045+171_1045+173delinsAGG ENSP00000420412.2:n.1045+171_1045+173delinsAGG
ENST00000489037.2:c.4279+171_4279+173delinsAGG ENSP00000420781.2:n.4279+171_4279+173delinsAGG
ENST00000493919.6:c.907+171_907+173delinsAGG ENSP00000418819.2:n.907+171_907+173delinsAGG
ENST00000494123.6:c.4357+171_4357+173delinsAGG ENSP00000419103.2:n.4357+171_4357+173delinsAGG
ENST00000497488.2:c.3469+171_3469+173delinsAGG ENSP00000418986.2:n.3469+171_3469+173delinsAGG
ENST00000618469.2:c.4357+171_4357+173delinsAGG ENSP00000478114.2:n.4357+171_4357+173delinsAGG
ENST00000634433.2:c.4234+171_4234+173delinsAGG ENSP00000489431.2:n.4234+171_4234+173delinsAGG
ENST00000644379.2:c.4357+171_4357+173delinsAGG ENSP00000496570.2:n.4357+171_4357+173delinsAGG
ENST00000644555.2:c.907+171_907+173delinsAGG ENSP00000494614.2:n.907+171_907+173delinsAGG
ENST00000652672.2:c.4216+171_4216+173delinsAGG ENSP00000498906.2:n.4216+171_4216+173delinsAGG
ENST00000484087.6:c.922+171_922+173delinsAGG ENSP00000419481.2:n.922+171_922+173delinsAGG
ENST00000700182.1:c.967+171_967+173delinsAGG ENSP00000514849.1:n.967+171_967+173delinsAGG
ENST00000357654.9:c.4357+171_4357+173delinsAGG MANE Select ENSP00000350283.3:n.4357+171_4357+173delinsAGG
ENST00000471181.7:c.4357+171_4357+173delinsAGG ENSP00000418960.2:n.4357+171_4357+173delinsAGG
ENST00000644379.1:c.678+171_678+173delinsAGG
ENST00000352993.7:c.931+171_931+173delinsAGG ENSP00000312236.5:n.931+171_931+173delinsAGG
ENST00000357654.7:c.4357+171_4357+173delinsAGG ENSP00000350283.3:n.4357+171_4357+173delinsAGG
ENST00000461221.5:c.*4140+171_*4140+173delinsAGG ENSP00000418548.1:n.*4140+171_*4140+173delinsAGG
ENST00000461574.1:c.651+171_651+173delinsAGG
ENST00000468300.5:c.1048+171_1048+173delinsAGG ENSP00000417148.1:n.1048+171_1048+173delinsAGG
ENST00000471181.6:c.4357+171_4357+173delinsAGG ENSP00000418960.2:n.4357+171_4357+173delinsAGG
ENST00000478531.5:c.1045+171_1045+173delinsAGG ENSP00000420412.1:n.1045+171_1045+173delinsAGG
ENST00000484087.5:c.670+171_670+173delinsAGG ENSP00000419481.1:n.670+171_670+173delinsAGG
ENST00000487825.5:c.673+171_673+173delinsAGG ENSP00000418212.1:n.673+171_673+173delinsAGG
ENST00000491747.6:c.1048+171_1048+173delinsAGG ENSP00000420705.2:n.1048+171_1048+173delinsAGG
ENST00000493795.5:c.4216+171_4216+173delinsAGG ENSP00000418775.1:n.4216+171_4216+173delinsAGG
ENST00000493919.5:c.907+171_907+173delinsAGG ENSP00000418819.1:n.907+171_907+173delinsAGG
ENST00000586385.5:c.5-18282_5-18280delinsAGG ENSP00000465818.1:n.5-18282_5-18280delinsAGG
ENST00000591534.5:c.-43-7712_-43-7710delinsAGG ENSP00000467329.1:n.-43-7712_-43-7710delinsAGG
ENST00000591849.5:c.-98-32043_-98-32041delinsAGG ENSP00000465347.1:n.-98-32043_-98-32041delinsAGG
ENST00000621897.1:n.251+171_251+173delinsAGG
NM_007294.3:c.4357+171_4357+173delinsAGG , LRG_292t1:c.4357+171_4357+173delinsAGG NP_009225.1:n.4357+171_4357+173delinsAGG
NM_007297.3:c.4216+171_4216+173delinsAGG NP_009228.2:n.4216+171_4216+173delinsAGG
NM_007298.3:c.1048+171_1048+173delinsAGG NP_009229.2:n.1048+171_1048+173delinsAGG
NM_007299.3:c.1048+171_1048+173delinsAGG NP_009230.2:n.1048+171_1048+173delinsAGG
NM_007300.3:c.4357+171_4357+173delinsAGG NP_009231.2:n.4357+171_4357+173delinsAGG
NR_027676.1:n.4493+171_4493+173delinsAGG
NM_007294.4:c.4357+171_4357+173delinsAGG MANE Select NP_009225.1:n.4357+171_4357+173delinsAGG
NM_007297.4:c.4216+171_4216+173delinsAGG NP_009228.2:n.4216+171_4216+173delinsAGG
NM_007299.4:c.1048+171_1048+173delinsAGG NP_009230.2:n.1048+171_1048+173delinsAGG
NM_007300.4:c.4357+171_4357+173delinsAGG NP_009231.2:n.4357+171_4357+173delinsAGG
NR_027676.2:n.4534+171_4534+173delinsAGG