Canonical Allele Identifier: CA2499224454
Gene: BRCA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1075602
ClinVar RCV Id: RCV001389229
dbSNP Id: rs80357687

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43091772_43091773insAA , CM000679.2:g.43091772_43091773insAA GRCh38
NC_000017.10:g.41243789_41243790insAA , CM000679.1:g.41243789_41243790insAA GRCh37
NC_000017.9:g.38497315_38497316insAA NCBI36
NG_005905.2:g.126212_126213insTT , LRG_292:g.126212_126213insTT

Transcript Alleles

HGVS Amino-acid change
ENST00000354071.8:n.3823_3824insTT
ENST00000461574.2:c.3759_3760insTT ENSP00000417241.2:p.Lys1254LeufsTer11
ENST00000470026.6:c.3759_3760insTT ENSP00000419274.2:p.Lys1254LeufsTer11
ENST00000473961.6:c.3633_3634insTT ENSP00000420201.2:p.Lys1212LeufsTer11
ENST00000476777.6:c.3756_3757insTT ENSP00000417554.2:p.Lys1253LeufsTer11
ENST00000477152.6:c.3681_3682insTT ENSP00000419988.2:p.Lys1228LeufsTer11
ENST00000478531.6:c.785-740_785-739insTT ENSP00000420412.2:n.785-740_785-739insTT
ENST00000489037.2:c.3681_3682insTT ENSP00000420781.2:p.Lys1228LeufsTer11
ENST00000493919.6:c.647-740_647-739insTT ENSP00000418819.2:n.647-740_647-739insTT
ENST00000494123.6:c.3759_3760insTT ENSP00000419103.2:p.Lys1254LeufsTer11
ENST00000497488.2:c.2871_2872insTT ENSP00000418986.2:p.Lys958LeufsTer11
ENST00000618469.2:c.3759_3760insTT ENSP00000478114.2:p.Lys1254LeufsTer11
ENST00000634433.2:c.3636_3637insTT ENSP00000489431.2:p.Lys1213LeufsTer11
ENST00000644379.2:c.3759_3760insTT ENSP00000496570.2:p.Lys1254LeufsTer11
ENST00000644555.2:c.647-740_647-739insTT ENSP00000494614.2:n.647-740_647-739insTT
ENST00000652672.2:c.3618_3619insTT ENSP00000498906.2:p.Lys1207LeufsTer11
ENST00000484087.6:c.665-740_665-739insTT ENSP00000419481.2:n.665-740_665-739insTT
ENST00000700182.1:c.707-740_707-739insTT ENSP00000514849.1:n.707-740_707-739insTT
ENST00000357654.9:c.3759_3760insTT MANE Select ENSP00000350283.3:p.Lys1254LeufsTer11
ENST00000471181.7:c.3759_3760insTT ENSP00000418960.2:p.Lys1254LeufsTer11
ENST00000644379.1:c.80_81insTT
ENST00000352993.7:c.671-740_671-739insTT ENSP00000312236.5:n.671-740_671-739insTT
ENST00000354071.7:c.3759_3760insTT ENSP00000326002.7:p.Lys1254LeufsTer11
ENST00000357654.7:c.3759_3760insTT ENSP00000350283.3:p.Lys1254LeufsTer11
ENST00000461221.5:c.*3542_*3543insTT ENSP00000418548.1:n.*3542_*3543insTT
ENST00000461574.1:c.53_54insTT
ENST00000468300.5:c.788-740_788-739insTT ENSP00000417148.1:n.788-740_788-739insTT
ENST00000471181.6:c.3759_3760insTT ENSP00000418960.2:p.Lys1254LeufsTer11
ENST00000478531.5:c.785-740_785-739insTT ENSP00000420412.1:n.785-740_785-739insTT
ENST00000484087.5:c.410-740_410-739insTT ENSP00000419481.1:n.410-740_410-739insTT
ENST00000487825.5:c.413-740_413-739insTT ENSP00000418212.1:n.413-740_413-739insTT
ENST00000491747.6:c.788-740_788-739insTT ENSP00000420705.2:n.788-740_788-739insTT
ENST00000493795.5:c.3618_3619insTT ENSP00000418775.1:p.Lys1207LeufsTer11
ENST00000493919.5:c.647-740_647-739insTT ENSP00000418819.1:n.647-740_647-739insTT
ENST00000586385.5:c.5-27821_5-27820insTT ENSP00000465818.1:n.5-27821_5-27820insTT
ENST00000591534.5:c.-43-17251_-43-17250insTT ENSP00000467329.1:n.-43-17251_-43-17250in...
ENST00000591849.5:c.-99+33499_-99+33500insTT ENSP00000465347.1:n.-99+33499_-99+33500in...
NM_007294.3:c.3759_3760insTT , LRG_292t1:c.3759_3760insTT NP_009225.1:p.Lys1254LeufsTer11
NM_007297.3:c.3618_3619insTT NP_009228.2:p.Lys1207LeufsTer11
NM_007298.3:c.788-740_788-739insTT NP_009229.2:n.788-740_788-739insTT
NM_007299.3:c.788-740_788-739insTT NP_009230.2:n.788-740_788-739insTT
NM_007300.3:c.3759_3760insTT NP_009231.2:p.Lys1254LeufsTer11
NR_027676.1:n.3895_3896insTT
NM_007294.4:c.3759_3760insTT MANE Select NP_009225.1:p.Lys1254LeufsTer11
NM_007297.4:c.3618_3619insTT NP_009228.2:p.Lys1207LeufsTer11
NM_007299.4:c.788-740_788-739insTT NP_009230.2:n.788-740_788-739insTT
NM_007300.4:c.3759_3760insTT NP_009231.2:p.Lys1254LeufsTer11
NR_027676.2:n.3936_3937insTT