Canonical Allele Identifier: CA2260775205
Gene: BRCA1 HGNC NCBI

Linked Data

dbSNP Id: rs2052691448

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43075946_43075951dup , CM000679.2:g.43075946_43075951dup GRCh38
NC_000017.10:g.41227963_41227968dup , CM000679.1:g.41227963_41227968dup GRCh37
NC_000017.9:g.38481489_38481494dup NCBI36
NG_005905.2:g.142033_142038dup , LRG_292:g.142033_142038dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000461574.2:c.4481+537_4481+542dup ENSP00000417241.2:n.4481+537_4481+542dup
ENST00000470026.6:c.4484+537_4484+542dup ENSP00000419274.2:n.4484+537_4484+542dup
ENST00000473961.6:c.4358+537_4358+542dup ENSP00000420201.2:n.4358+537_4358+542dup
ENST00000476777.6:c.4478+537_4478+542dup ENSP00000417554.2:n.4478+537_4478+542dup
ENST00000477152.6:c.4406+537_4406+542dup ENSP00000419988.2:n.4406+537_4406+542dup
ENST00000478531.6:c.1172+537_1172+542dup ENSP00000420412.2:n.1172+537_1172+542dup
ENST00000489037.2:c.4406+537_4406+542dup ENSP00000420781.2:n.4406+537_4406+542dup
ENST00000493919.6:c.1034+537_1034+542dup ENSP00000418819.2:n.1034+537_1034+542dup
ENST00000494123.6:c.4484+537_4484+542dup ENSP00000419103.2:n.4484+537_4484+542dup
ENST00000497488.2:c.3596+537_3596+542dup ENSP00000418986.2:n.3596+537_3596+542dup
ENST00000618469.2:c.4484+537_4484+542dup ENSP00000478114.2:n.4484+537_4484+542dup
ENST00000634433.2:c.4361+537_4361+542dup ENSP00000489431.2:n.4361+537_4361+542dup
ENST00000644379.2:c.4550+537_4550+542dup ENSP00000496570.2:n.4550+537_4550+542dup
ENST00000644555.2:c.1034+537_1034+542dup ENSP00000494614.2:n.1034+537_1034+542dup
ENST00000652672.2:c.4343+537_4343+542dup ENSP00000498906.2:n.4343+537_4343+542dup
ENST00000484087.6:c.1046+537_1046+542dup ENSP00000419481.2:n.1046+537_1046+542dup
ENST00000700182.1:c.1091+537_1091+542dup ENSP00000514849.1:n.1091+537_1091+542dup
ENST00000357654.9:c.4484+537_4484+542dup MANE Select ENSP00000350283.3:n.4484+537_4484+542dup
ENST00000471181.7:c.4547+537_4547+542dup ENSP00000418960.2:n.4547+537_4547+542dup
ENST00000644379.1:c.871+537_871+542dup
ENST00000352993.7:c.1058+537_1058+542dup ENSP00000312236.5:n.1058+537_1058+542dup
ENST00000357654.7:c.4484+537_4484+542dup ENSP00000350283.3:n.4484+537_4484+542dup
ENST00000461221.5:c.*4267+537_*4267+542dup ENSP00000418548.1:n.*4267+537_*4267+542dup
ENST00000468300.5:c.1172+537_1172+542dup ENSP00000417148.1:n.1172+537_1172+542dup
ENST00000471181.6:c.4547+537_4547+542dup ENSP00000418960.2:n.4547+537_4547+542dup
ENST00000478531.5:c.1172+537_1172+542dup ENSP00000420412.1:n.1172+537_1172+542dup
ENST00000484087.5:c.797+537_797+542dup ENSP00000419481.1:n.797+537_797+542dup
ENST00000491747.6:c.1172+537_1172+542dup ENSP00000420705.2:n.1172+537_1172+542dup
ENST00000493795.5:c.4343+537_4343+542dup ENSP00000418775.1:n.4343+537_4343+542dup
ENST00000493919.5:c.1034+537_1034+542dup ENSP00000418819.1:n.1034+537_1034+542dup
ENST00000586385.5:c.5-12000_5-11995dup ENSP00000465818.1:n.5-12000_5-11995dup
ENST00000591534.5:c.-43-1430_-43-1425dup ENSP00000467329.1:n.-43-1430_-43-1425dup
ENST00000591849.5:c.-98-25761_-98-25756dup ENSP00000465347.1:n.-98-25761_-98-25756dup
NM_007294.3:c.4484+537_4484+542dup , LRG_292t1:c.4484+537_4484+542dup NP_009225.1:n.4484+537_4484+542dup
NM_007297.3:c.4343+537_4343+542dup NP_009228.2:n.4343+537_4343+542dup
NM_007298.3:c.1172+537_1172+542dup NP_009229.2:n.1172+537_1172+542dup
NM_007299.3:c.1172+537_1172+542dup NP_009230.2:n.1172+537_1172+542dup
NM_007300.3:c.4547+537_4547+542dup NP_009231.2:n.4547+537_4547+542dup
NR_027676.1:n.4620+537_4620+542dup
NM_007294.4:c.4484+537_4484+542dup MANE Select NP_009225.1:n.4484+537_4484+542dup
NM_007297.4:c.4343+537_4343+542dup NP_009228.2:n.4343+537_4343+542dup
NM_007299.4:c.1172+537_1172+542dup NP_009230.2:n.1172+537_1172+542dup
NM_007300.4:c.4547+537_4547+542dup NP_009231.2:n.4547+537_4547+542dup
NR_027676.2:n.4661+537_4661+542dup