Canonical Allele Identifier: CA2638062121
Gene: BRCA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43067786_43067787insCG , CM000679.2:g.43067786_43067787insCG GRCh38
NC_000017.10:g.41219803_41219804insCG , CM000679.1:g.41219803_41219804insCG GRCh37
NC_000017.9:g.38473329_38473330insCG NCBI36
NG_005905.2:g.150197_150198insCG , LRG_292:g.150197_150198insCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000461574.2:c.4984-92_4984-91insCG ENSP00000417241.2:n.4984-92_4984-91insCG
ENST00000470026.6:c.4987-92_4987-91insCG ENSP00000419274.2:n.4987-92_4987-91insCG
ENST00000473961.6:c.4861-92_4861-91insCG ENSP00000420201.2:n.4861-92_4861-91insCG
ENST00000476777.6:c.4981-92_4981-91insCG ENSP00000417554.2:n.4981-92_4981-91insCG
ENST00000477152.6:c.4909-92_4909-91insCG ENSP00000419988.2:n.4909-92_4909-91insCG
ENST00000478531.6:c.1675-92_1675-91insCG ENSP00000420412.2:n.1675-92_1675-91insCG
ENST00000489037.2:c.4909-92_4909-91insCG ENSP00000420781.2:n.4909-92_4909-91insCG
ENST00000493919.6:c.1537-92_1537-91insCG ENSP00000418819.2:n.1537-92_1537-91insCG
ENST00000494123.6:c.4987-92_4987-91insCG ENSP00000419103.2:n.4987-92_4987-91insCG
ENST00000497488.2:c.4099-92_4099-91insCG ENSP00000418986.2:n.4099-92_4099-91insCG
ENST00000618469.2:c.4987-92_4987-91insCG ENSP00000478114.2:n.4987-92_4987-91insCG
ENST00000634433.2:c.4864-92_4864-91insCG ENSP00000489431.2:n.4864-92_4864-91insCG
ENST00000644379.2:c.5053-92_5053-91insCG ENSP00000496570.2:n.5053-92_5053-91insCG
ENST00000644555.2:c.1537-92_1537-91insCG ENSP00000494614.2:n.1537-92_1537-91insCG
ENST00000652672.2:c.4846-92_4846-91insCG ENSP00000498906.2:n.4846-92_4846-91insCG
ENST00000484087.6:c.1549-92_1549-91insCG ENSP00000419481.2:n.1549-92_1549-91insCG
ENST00000357654.9:c.4987-92_4987-91insCG MANE Select ENSP00000350283.3:n.4987-92_4987-91insCG
ENST00000471181.7:c.5050-92_5050-91insCG ENSP00000418960.2:n.5050-92_5050-91insCG
ENST00000644379.1:c.1374-92_1374-91insCG
ENST00000352993.7:c.1561-92_1561-91insCG ENSP00000312236.5:n.1561-92_1561-91insCG
ENST00000357654.7:c.4987-92_4987-91insCG ENSP00000350283.3:n.4987-92_4987-91insCG
ENST00000461221.5:c.*4770-92_*4770-91insCG ENSP00000418548.1:n.*4770-92_*4770-91insCG
ENST00000468300.5:c.1675-92_1675-91insCG ENSP00000417148.1:n.1675-92_1675-91insCG
ENST00000471181.6:c.5050-92_5050-91insCG ENSP00000418960.2:n.5050-92_5050-91insCG
ENST00000472490.1:n.140-92_140-91insCG
ENST00000478531.5:c.1675-92_1675-91insCG ENSP00000420412.1:n.1675-92_1675-91insCG
ENST00000484087.5:c.1300-92_1300-91insCG ENSP00000419481.1:n.1300-92_1300-91insCG
ENST00000491747.6:c.1675-92_1675-91insCG ENSP00000420705.2:n.1675-92_1675-91insCG
ENST00000493795.5:c.4846-92_4846-91insCG ENSP00000418775.1:n.4846-92_4846-91insCG
ENST00000493919.5:c.1537-92_1537-91insCG ENSP00000418819.1:n.1537-92_1537-91insCG
ENST00000586385.5:c.5-3836_5-3835insCG ENSP00000465818.1:n.5-3836_5-3835insCG
ENST00000591534.5:c.460-92_460-91insCG ENSP00000467329.1:n.460-92_460-91insCG
ENST00000591849.5:c.-98-17597_-98-17596insCG ENSP00000465347.1:n.-98-17597_-98-17596insCG
NM_007294.3:c.4987-92_4987-91insCG , LRG_292t1:c.4987-92_4987-91insCG NP_009225.1:n.4987-92_4987-91insCG
NM_007297.3:c.4846-92_4846-91insCG NP_009228.2:n.4846-92_4846-91insCG
NM_007298.3:c.1675-92_1675-91insCG NP_009229.2:n.1675-92_1675-91insCG
NM_007299.3:c.1675-92_1675-91insCG NP_009230.2:n.1675-92_1675-91insCG
NM_007300.3:c.5050-92_5050-91insCG NP_009231.2:n.5050-92_5050-91insCG
NR_027676.1:n.5123-92_5123-91insCG
NM_007294.4:c.4987-92_4987-91insCG MANE Select NP_009225.1:n.4987-92_4987-91insCG
NM_007297.4:c.4846-92_4846-91insCG NP_009228.2:n.4846-92_4846-91insCG
NM_007299.4:c.1675-92_1675-91insCG NP_009230.2:n.1675-92_1675-91insCG
NM_007300.4:c.5050-92_5050-91insCG NP_009231.2:n.5050-92_5050-91insCG
NR_027676.2:n.5164-92_5164-91insCG