Canonical Allele Identifier: CA003936
Gene: BRCA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 186539
dbSNP Id: rs786203027

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43094686G>A , CM000679.2:g.43094686G>A GRCh38
NC_000017.10:g.41246703G>A , CM000679.1:g.41246703G>A GRCh37
NC_000017.9:g.38500229G>A NCBI36
NG_005905.2:g.123298C>T , LRG_292:g.123298C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000354071.8:n.909C>T
ENST00000461574.2:c.845C>T ENSP00000417241.2:p.Ser282Leu
ENST00000470026.6:c.845C>T ENSP00000419274.2:p.Ser282Leu
ENST00000473961.6:c.719C>T ENSP00000420201.2:p.Ser240Leu
ENST00000476777.6:c.842C>T ENSP00000417554.2:p.Ser281Leu
ENST00000477152.6:c.767C>T ENSP00000419988.2:p.Ser256Leu
ENST00000478531.6:c.784+58C>T ENSP00000420412.2:n.784+58C>T
ENST00000489037.2:c.767C>T ENSP00000420781.2:p.Ser256Leu
ENST00000493919.6:c.646+58C>T ENSP00000418819.2:n.646+58C>T
ENST00000494123.6:c.845C>T ENSP00000419103.2:p.Ser282Leu
ENST00000497488.2:c.-44C>T ENSP00000418986.2:n.-44C>T
ENST00000618469.2:c.845C>T ENSP00000478114.2:p.Ser282Leu
ENST00000634433.2:c.722C>T ENSP00000489431.2:p.Ser241Leu
ENST00000644379.2:c.845C>T ENSP00000496570.2:p.Ser282Leu
ENST00000644555.2:c.646+58C>T ENSP00000494614.2:n.646+58C>T
ENST00000652672.2:c.704C>T ENSP00000498906.2:p.Ser235Leu
ENST00000484087.6:c.664+58C>T ENSP00000419481.2:n.664+58C>T
ENST00000700182.1:c.706+58C>T ENSP00000514849.1:n.706+58C>T
ENST00000700183.1:c.*853C>T ENSP00000514850.1:n.*853C>T
ENST00000357654.9:c.845C>T MANE Select ENSP00000350283.3:p.Ser282Leu
ENST00000471181.7:c.845C>T ENSP00000418960.2:p.Ser282Leu
ENST00000642945.1:c.*719C>T ENSP00000495897.1:n.*719C>T
ENST00000652672.1:c.704C>T ENSP00000498906.1:p.Ser235Leu
ENST00000352993.7:c.670+1160C>T ENSP00000312236.5:n.670+1160C>T
ENST00000354071.7:c.845C>T ENSP00000326002.7:p.Ser282Leu
ENST00000357654.7:c.845C>T ENSP00000350283.3:p.Ser282Leu
ENST00000412061.3:c.196C>T
ENST00000461221.5:c.*628C>T ENSP00000418548.1:n.*628C>T
ENST00000468300.5:c.787+58C>T ENSP00000417148.1:n.787+58C>T
ENST00000470026.5:c.845C>T ENSP00000419274.1:p.Ser282Leu
ENST00000471181.6:c.845C>T ENSP00000418960.2:p.Ser282Leu
ENST00000473961.5:c.442C>T
ENST00000477152.5:c.767C>T ENSP00000419988.1:p.Ser256Leu
ENST00000478531.5:c.784+58C>T ENSP00000420412.1:n.784+58C>T
ENST00000484087.5:c.409+58C>T ENSP00000419481.1:n.409+58C>T
ENST00000487825.5:c.412+58C>T ENSP00000418212.1:n.412+58C>T
ENST00000491747.6:c.787+58C>T ENSP00000420705.2:n.787+58C>T
ENST00000492859.5:c.*781C>T ENSP00000420253.1:n.*781C>T
ENST00000493795.5:c.704C>T ENSP00000418775.1:p.Ser235Leu
ENST00000493919.5:c.646+58C>T ENSP00000418819.1:n.646+58C>T
ENST00000494123.5:c.845C>T ENSP00000419103.1:p.Ser282Leu
ENST00000497488.1:c.-44C>T ENSP00000418986.1:n.-44C>T
ENST00000586385.5:c.4+30496C>T ENSP00000465818.1:n.4+30496C>T
ENST00000591534.5:c.-43-20165C>T ENSP00000467329.1:n.-43-20165C>T
ENST00000591849.5:c.-99+30585C>T ENSP00000465347.1:n.-99+30585C>T
ENST00000634433.1:c.722C>T ENSP00000489431.1:p.Ser241Leu
NM_007294.3:c.845C>T , LRG_292t1:c.845C>T NP_009225.1:p.Ser282Leu
NM_007297.3:c.704C>T NP_009228.2:p.Ser235Leu
NM_007298.3:c.787+58C>T NP_009229.2:n.787+58C>T
NM_007299.3:c.787+58C>T NP_009230.2:n.787+58C>T
NM_007300.3:c.845C>T NP_009231.2:p.Ser282Leu
NR_027676.1:n.981C>T
NM_007294.4:c.845C>T MANE Select NP_009225.1:p.Ser282Leu
NM_007297.4:c.704C>T NP_009228.2:p.Ser235Leu
NM_007299.4:c.787+58C>T NP_009230.2:n.787+58C>T
NM_007300.4:c.845C>T NP_009231.2:p.Ser282Leu
NR_027676.2:n.1022C>T