Canonical Allele Identifier: CA2260777805
Gene: BRCA1 HGNC NCBI

Linked Data

dbSNP Id: rs2053023531

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43082053_43082054del , CM000679.2:g.43082053_43082054del GRCh38
NC_000017.10:g.41234070_41234071del , CM000679.1:g.41234070_41234071del GRCh37
NC_000017.9:g.38487596_38487597del NCBI36
NG_005905.2:g.135930_135931del , LRG_292:g.135930_135931del

Transcript Alleles

HGVS Amino-acid Change
ENST00000461574.2:c.4357+350_4357+351del ENSP00000417241.2:n.4357+350_4357+351del
ENST00000470026.6:c.4357+350_4357+351del ENSP00000419274.2:n.4357+350_4357+351del
ENST00000473961.6:c.4231+350_4231+351del ENSP00000420201.2:n.4231+350_4231+351del
ENST00000476777.6:c.4351+350_4351+351del ENSP00000417554.2:n.4351+350_4351+351del
ENST00000477152.6:c.4279+350_4279+351del ENSP00000419988.2:n.4279+350_4279+351del
ENST00000478531.6:c.1045+350_1045+351del ENSP00000420412.2:n.1045+350_1045+351del
ENST00000489037.2:c.4279+350_4279+351del ENSP00000420781.2:n.4279+350_4279+351del
ENST00000493919.6:c.907+350_907+351del ENSP00000418819.2:n.907+350_907+351del
ENST00000494123.6:c.4357+350_4357+351del ENSP00000419103.2:n.4357+350_4357+351del
ENST00000497488.2:c.3469+350_3469+351del ENSP00000418986.2:n.3469+350_3469+351del
ENST00000618469.2:c.4357+350_4357+351del ENSP00000478114.2:n.4357+350_4357+351del
ENST00000634433.2:c.4234+350_4234+351del ENSP00000489431.2:n.4234+350_4234+351del
ENST00000644379.2:c.4357+350_4357+351del ENSP00000496570.2:n.4357+350_4357+351del
ENST00000644555.2:c.907+350_907+351del ENSP00000494614.2:n.907+350_907+351del
ENST00000652672.2:c.4216+350_4216+351del ENSP00000498906.2:n.4216+350_4216+351del
ENST00000484087.6:c.922+350_922+351del ENSP00000419481.2:n.922+350_922+351del
ENST00000700182.1:c.967+350_967+351del ENSP00000514849.1:n.967+350_967+351del
ENST00000357654.9:c.4357+350_4357+351del MANE Select ENSP00000350283.3:n.4357+350_4357+351del
ENST00000471181.7:c.4357+350_4357+351del ENSP00000418960.2:n.4357+350_4357+351del
ENST00000644379.1:c.678+350_678+351del
ENST00000352993.7:c.931+350_931+351del ENSP00000312236.5:n.931+350_931+351del
ENST00000357654.7:c.4357+350_4357+351del ENSP00000350283.3:n.4357+350_4357+351del
ENST00000461221.5:c.*4140+350_*4140+351del ENSP00000418548.1:n.*4140+350_*4140+351del
ENST00000461574.1:c.651+350_651+351del
ENST00000468300.5:c.1048+350_1048+351del ENSP00000417148.1:n.1048+350_1048+351del
ENST00000471181.6:c.4357+350_4357+351del ENSP00000418960.2:n.4357+350_4357+351del
ENST00000478531.5:c.1045+350_1045+351del ENSP00000420412.1:n.1045+350_1045+351del
ENST00000484087.5:c.670+350_670+351del ENSP00000419481.1:n.670+350_670+351del
ENST00000487825.5:c.673+350_673+351del ENSP00000418212.1:n.673+350_673+351del
ENST00000491747.6:c.1048+350_1048+351del ENSP00000420705.2:n.1048+350_1048+351del
ENST00000493795.5:c.4216+350_4216+351del ENSP00000418775.1:n.4216+350_4216+351del
ENST00000493919.5:c.907+350_907+351del ENSP00000418819.1:n.907+350_907+351del
ENST00000586385.5:c.5-18103_5-18102del ENSP00000465818.1:n.5-18103_5-18102del
ENST00000591534.5:c.-43-7533_-43-7532del ENSP00000467329.1:n.-43-7533_-43-7532del
ENST00000591849.5:c.-98-31864_-98-31863del ENSP00000465347.1:n.-98-31864_-98-31863del
ENST00000621897.1:n.251+350_251+351del
NM_007294.3:c.4357+350_4357+351del , LRG_292t1:c.4357+350_4357+351del NP_009225.1:n.4357+350_4357+351del
NM_007297.3:c.4216+350_4216+351del NP_009228.2:n.4216+350_4216+351del
NM_007298.3:c.1048+350_1048+351del NP_009229.2:n.1048+350_1048+351del
NM_007299.3:c.1048+350_1048+351del NP_009230.2:n.1048+350_1048+351del
NM_007300.3:c.4357+350_4357+351del NP_009231.2:n.4357+350_4357+351del
NR_027676.1:n.4493+350_4493+351del
NM_007294.4:c.4357+350_4357+351del MANE Select NP_009225.1:n.4357+350_4357+351del
NM_007297.4:c.4216+350_4216+351del NP_009228.2:n.4216+350_4216+351del
NM_007299.4:c.1048+350_1048+351del NP_009230.2:n.1048+350_1048+351del
NM_007300.4:c.4357+350_4357+351del NP_009231.2:n.4357+350_4357+351del
NR_027676.2:n.4534+350_4534+351del