Canonical Allele Identifier: CA002485
Gene: BRCA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 187761
dbSNP Id: rs142383077

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43091674C>G , CM000679.2:g.43091674C>G GRCh38
NC_000017.10:g.41243691C>G , CM000679.1:g.41243691C>G GRCh37
NC_000017.9:g.38497217C>G NCBI36
NG_005905.2:g.126310G>C , LRG_292:g.126310G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000354071.8:n.3921G>C
ENST00000461574.2:c.3857G>C ENSP00000417241.2:p.Ser1286Thr
ENST00000470026.6:c.3857G>C ENSP00000419274.2:p.Ser1286Thr
ENST00000473961.6:c.3731G>C ENSP00000420201.2:p.Ser1244Thr
ENST00000476777.6:c.3854G>C ENSP00000417554.2:p.Ser1285Thr
ENST00000477152.6:c.3779G>C ENSP00000419988.2:p.Ser1260Thr
ENST00000478531.6:c.785-642G>C ENSP00000420412.2:n.785-642G>C
ENST00000489037.2:c.3779G>C ENSP00000420781.2:p.Ser1260Thr
ENST00000493919.6:c.647-642G>C ENSP00000418819.2:n.647-642G>C
ENST00000494123.6:c.3857G>C ENSP00000419103.2:p.Ser1286Thr
ENST00000497488.2:c.2969G>C ENSP00000418986.2:p.Ser990Thr
ENST00000618469.2:c.3857G>C ENSP00000478114.2:p.Ser1286Thr
ENST00000634433.2:c.3734G>C ENSP00000489431.2:p.Ser1245Thr
ENST00000644379.2:c.3857G>C ENSP00000496570.2:p.Ser1286Thr
ENST00000644555.2:c.647-642G>C ENSP00000494614.2:n.647-642G>C
ENST00000652672.2:c.3716G>C ENSP00000498906.2:p.Ser1239Thr
ENST00000484087.6:c.665-642G>C ENSP00000419481.2:n.665-642G>C
ENST00000700182.1:c.707-642G>C ENSP00000514849.1:n.707-642G>C
ENST00000357654.9:c.3857G>C MANE Select ENSP00000350283.3:p.Ser1286Thr
ENST00000471181.7:c.3857G>C ENSP00000418960.2:p.Ser1286Thr
ENST00000644379.1:c.178G>C
ENST00000352993.7:c.671-642G>C ENSP00000312236.5:n.671-642G>C
ENST00000354071.7:c.3857G>C ENSP00000326002.7:p.Ser1286Thr
ENST00000357654.7:c.3857G>C ENSP00000350283.3:p.Ser1286Thr
ENST00000461221.5:c.*3640G>C ENSP00000418548.1:n.*3640G>C
ENST00000461574.1:c.151G>C
ENST00000468300.5:c.788-642G>C ENSP00000417148.1:n.788-642G>C
ENST00000471181.6:c.3857G>C ENSP00000418960.2:p.Ser1286Thr
ENST00000478531.5:c.785-642G>C ENSP00000420412.1:n.785-642G>C
ENST00000484087.5:c.410-642G>C ENSP00000419481.1:n.410-642G>C
ENST00000487825.5:c.413-642G>C ENSP00000418212.1:n.413-642G>C
ENST00000491747.6:c.788-642G>C ENSP00000420705.2:n.788-642G>C
ENST00000493795.5:c.3716G>C ENSP00000418775.1:p.Ser1239Thr
ENST00000493919.5:c.647-642G>C ENSP00000418819.1:n.647-642G>C
ENST00000586385.5:c.5-27723G>C ENSP00000465818.1:n.5-27723G>C
ENST00000591534.5:c.-43-17153G>C ENSP00000467329.1:n.-43-17153G>C
ENST00000591849.5:c.-99+33597G>C ENSP00000465347.1:n.-99+33597G>C
NM_007294.3:c.3857G>C , LRG_292t1:c.3857G>C NP_009225.1:p.Ser1286Thr
NM_007297.3:c.3716G>C NP_009228.2:p.Ser1239Thr
NM_007298.3:c.788-642G>C NP_009229.2:n.788-642G>C
NM_007299.3:c.788-642G>C NP_009230.2:n.788-642G>C
NM_007300.3:c.3857G>C NP_009231.2:p.Ser1286Thr
NR_027676.1:n.3993G>C
NM_007294.4:c.3857G>C MANE Select NP_009225.1:p.Ser1286Thr
NM_007297.4:c.3716G>C NP_009228.2:p.Ser1239Thr
NM_007299.4:c.788-642G>C NP_009230.2:n.788-642G>C
NM_007300.4:c.3857G>C NP_009231.2:p.Ser1286Thr
NR_027676.2:n.4034G>C