Canonical Allele Identifier: CA10594092
Gene: BRCA1 HGNC NCBI

Linked Data

dbSNP Id: rs878995408

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43091597T>A , CM000679.2:g.43091597T>A GRCh38
NC_000017.10:g.41243614T>A , CM000679.1:g.41243614T>A GRCh37
NC_000017.9:g.38497140T>A NCBI36
NG_005905.2:g.126387A>T , LRG_292:g.126387A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000354071.8:n.3998A>T
ENST00000461574.2:c.3934A>T ENSP00000417241.2:p.Thr1312Ser
ENST00000470026.6:c.3934A>T ENSP00000419274.2:p.Thr1312Ser
ENST00000473961.6:c.3808A>T ENSP00000420201.2:p.Thr1270Ser
ENST00000476777.6:c.3931A>T ENSP00000417554.2:p.Thr1311Ser
ENST00000477152.6:c.3856A>T ENSP00000419988.2:p.Thr1286Ser
ENST00000478531.6:c.785-565A>T ENSP00000420412.2:n.785-565A>T
ENST00000489037.2:c.3856A>T ENSP00000420781.2:p.Thr1286Ser
ENST00000493919.6:c.647-565A>T ENSP00000418819.2:n.647-565A>T
ENST00000494123.6:c.3934A>T ENSP00000419103.2:p.Thr1312Ser
ENST00000497488.2:c.3046A>T ENSP00000418986.2:p.Thr1016Ser
ENST00000618469.2:c.3934A>T ENSP00000478114.2:p.Thr1312Ser
ENST00000634433.2:c.3811A>T ENSP00000489431.2:p.Thr1271Ser
ENST00000644379.2:c.3934A>T ENSP00000496570.2:p.Thr1312Ser
ENST00000644555.2:c.647-565A>T ENSP00000494614.2:n.647-565A>T
ENST00000652672.2:c.3793A>T ENSP00000498906.2:p.Thr1265Ser
ENST00000484087.6:c.665-565A>T ENSP00000419481.2:n.665-565A>T
ENST00000700182.1:c.707-565A>T ENSP00000514849.1:n.707-565A>T
ENST00000357654.9:c.3934A>T MANE Select ENSP00000350283.3:p.Thr1312Ser
ENST00000471181.7:c.3934A>T ENSP00000418960.2:p.Thr1312Ser
ENST00000644379.1:c.255A>T
ENST00000352993.7:c.671-565A>T ENSP00000312236.5:n.671-565A>T
ENST00000354071.7:c.3934A>T ENSP00000326002.7:p.Thr1312Ser
ENST00000357654.7:c.3934A>T ENSP00000350283.3:p.Thr1312Ser
ENST00000461221.5:c.*3717A>T ENSP00000418548.1:n.*3717A>T
ENST00000461574.1:c.228A>T
ENST00000468300.5:c.788-565A>T ENSP00000417148.1:n.788-565A>T
ENST00000471181.6:c.3934A>T ENSP00000418960.2:p.Thr1312Ser
ENST00000478531.5:c.785-565A>T ENSP00000420412.1:n.785-565A>T
ENST00000484087.5:c.410-565A>T ENSP00000419481.1:n.410-565A>T
ENST00000487825.5:c.413-565A>T ENSP00000418212.1:n.413-565A>T
ENST00000491747.6:c.788-565A>T ENSP00000420705.2:n.788-565A>T
ENST00000493795.5:c.3793A>T ENSP00000418775.1:p.Thr1265Ser
ENST00000493919.5:c.647-565A>T ENSP00000418819.1:n.647-565A>T
ENST00000586385.5:c.5-27646A>T ENSP00000465818.1:n.5-27646A>T
ENST00000591534.5:c.-43-17076A>T ENSP00000467329.1:n.-43-17076A>T
ENST00000591849.5:c.-99+33674A>T ENSP00000465347.1:n.-99+33674A>T
NM_007294.3:c.3934A>T , LRG_292t1:c.3934A>T NP_009225.1:p.Thr1312Ser
NM_007297.3:c.3793A>T NP_009228.2:p.Thr1265Ser
NM_007298.3:c.788-565A>T NP_009229.2:n.788-565A>T
NM_007299.3:c.788-565A>T NP_009230.2:n.788-565A>T
NM_007300.3:c.3934A>T NP_009231.2:p.Thr1312Ser
NR_027676.1:n.4070A>T
NM_007294.4:c.3934A>T MANE Select NP_009225.1:p.Thr1312Ser
NM_007297.4:c.3793A>T NP_009228.2:p.Thr1265Ser
NM_007299.4:c.788-565A>T NP_009230.2:n.788-565A>T
NM_007300.4:c.3934A>T NP_009231.2:p.Thr1312Ser
NR_027676.2:n.4111A>T