Canonical Allele Identifier: CA2260775395
Gene: BRCA1 HGNC NCBI

Linked Data

dbSNP Id: rs2052711774

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43076400_43076401insC , CM000679.2:g.43076400_43076401insC GRCh38
NC_000017.10:g.41228417_41228418insC , CM000679.1:g.41228417_41228418insC GRCh37
NC_000017.9:g.38481943_38481944insC NCBI36
NG_005905.2:g.141583_141584insG , LRG_292:g.141583_141584insG

Transcript Alleles

HGVS Amino-acid change
ENST00000461574.2:c.4481+87_4481+88insG ENSP00000417241.2:n.4481+87_4481+88insG
ENST00000470026.6:c.4484+87_4484+88insG ENSP00000419274.2:n.4484+87_4484+88insG
ENST00000473961.6:c.4358+87_4358+88insG ENSP00000420201.2:n.4358+87_4358+88insG
ENST00000476777.6:c.4478+87_4478+88insG ENSP00000417554.2:n.4478+87_4478+88insG
ENST00000477152.6:c.4406+87_4406+88insG ENSP00000419988.2:n.4406+87_4406+88insG
ENST00000478531.6:c.1172+87_1172+88insG ENSP00000420412.2:n.1172+87_1172+88insG
ENST00000489037.2:c.4406+87_4406+88insG ENSP00000420781.2:n.4406+87_4406+88insG
ENST00000493919.6:c.1034+87_1034+88insG ENSP00000418819.2:n.1034+87_1034+88insG
ENST00000494123.6:c.4484+87_4484+88insG ENSP00000419103.2:n.4484+87_4484+88insG
ENST00000497488.2:c.3596+87_3596+88insG ENSP00000418986.2:n.3596+87_3596+88insG
ENST00000618469.2:c.4484+87_4484+88insG ENSP00000478114.2:n.4484+87_4484+88insG
ENST00000634433.2:c.4361+87_4361+88insG ENSP00000489431.2:n.4361+87_4361+88insG
ENST00000644379.2:c.4550+87_4550+88insG ENSP00000496570.2:n.4550+87_4550+88insG
ENST00000644555.2:c.1034+87_1034+88insG ENSP00000494614.2:n.1034+87_1034+88insG
ENST00000652672.2:c.4343+87_4343+88insG ENSP00000498906.2:n.4343+87_4343+88insG
ENST00000484087.6:c.1046+87_1046+88insG ENSP00000419481.2:n.1046+87_1046+88insG
ENST00000700182.1:c.1091+87_1091+88insG ENSP00000514849.1:n.1091+87_1091+88insG
ENST00000357654.9:c.4484+87_4484+88insG MANE Select ENSP00000350283.3:n.4484+87_4484+88insG
ENST00000471181.7:c.4547+87_4547+88insG ENSP00000418960.2:n.4547+87_4547+88insG
ENST00000644379.1:c.871+87_871+88insG
ENST00000352993.7:c.1058+87_1058+88insG ENSP00000312236.5:n.1058+87_1058+88insG
ENST00000357654.7:c.4484+87_4484+88insG ENSP00000350283.3:n.4484+87_4484+88insG
ENST00000461221.5:c.*4267+87_*4267+88insG ENSP00000418548.1:n.*4267+87_*4267+88insG
ENST00000468300.5:c.1172+87_1172+88insG ENSP00000417148.1:n.1172+87_1172+88insG
ENST00000471181.6:c.4547+87_4547+88insG ENSP00000418960.2:n.4547+87_4547+88insG
ENST00000478531.5:c.1172+87_1172+88insG ENSP00000420412.1:n.1172+87_1172+88insG
ENST00000484087.5:c.797+87_797+88insG ENSP00000419481.1:n.797+87_797+88insG
ENST00000491747.6:c.1172+87_1172+88insG ENSP00000420705.2:n.1172+87_1172+88insG
ENST00000493795.5:c.4343+87_4343+88insG ENSP00000418775.1:n.4343+87_4343+88insG
ENST00000493919.5:c.1034+87_1034+88insG ENSP00000418819.1:n.1034+87_1034+88insG
ENST00000586385.5:c.5-12450_5-12449insG ENSP00000465818.1:n.5-12450_5-12449insG
ENST00000591534.5:c.-43-1880_-43-1879insG ENSP00000467329.1:n.-43-1880_-43-1879insG
ENST00000591849.5:c.-98-26211_-98-26210insG ENSP00000465347.1:n.-98-26211_-98-26210insG
NM_007294.3:c.4484+87_4484+88insG , LRG_292t1:c.4484+87_4484+88insG NP_009225.1:n.4484+87_4484+88insG
NM_007297.3:c.4343+87_4343+88insG NP_009228.2:n.4343+87_4343+88insG
NM_007298.3:c.1172+87_1172+88insG NP_009229.2:n.1172+87_1172+88insG
NM_007299.3:c.1172+87_1172+88insG NP_009230.2:n.1172+87_1172+88insG
NM_007300.3:c.4547+87_4547+88insG NP_009231.2:n.4547+87_4547+88insG
NR_027676.1:n.4620+87_4620+88insG
NM_007294.4:c.4484+87_4484+88insG MANE Select NP_009225.1:n.4484+87_4484+88insG
NM_007297.4:c.4343+87_4343+88insG NP_009228.2:n.4343+87_4343+88insG
NM_007299.4:c.1172+87_1172+88insG NP_009230.2:n.1172+87_1172+88insG
NM_007300.4:c.4547+87_4547+88insG NP_009231.2:n.4547+87_4547+88insG
NR_027676.2:n.4661+87_4661+88insG