Canonical Allele Identifier: CA2260782273
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43091775_43091777delinsCAG , CM000679.2:g.43091775_43091777delinsCAG GRCh38
NC_000017.10:g.41243792_41243794delinsCAG , CM000679.1:g.41243792_41243794delinsCAG GRCh37
NC_000017.9:g.38497318_38497320delinsCAG NCBI36
NG_005905.2:g.126207_126209delinsCTG , LRG_292:g.126207_126209delinsCTG

Transcript Alleles

HGVS Amino-acid change
ENST00000354071.8:n.3818_3820delinsCTG
ENST00000461574.2:c.3754_3756delinsCTG ENSP00000417241.2:p.Leu1252=
ENST00000470026.6:c.3754_3756delinsCTG ENSP00000419274.2:p.Leu1252=
ENST00000473961.6:c.3628_3630delinsCTG ENSP00000420201.2:p.Leu1210=
ENST00000476777.6:c.3751_3753delinsCTG ENSP00000417554.2:p.Leu1251=
ENST00000477152.6:c.3676_3678delinsCTG ENSP00000419988.2:p.Leu1226=
ENST00000478531.6:c.785-745_785-743delinsCTG ENSP00000420412.2:n.785-745_785-743delins...
ENST00000489037.2:c.3676_3678delinsCTG ENSP00000420781.2:p.Leu1226=
ENST00000493919.6:c.647-745_647-743delinsCTG ENSP00000418819.2:n.647-745_647-743delins...
ENST00000494123.6:c.3754_3756delinsCTG ENSP00000419103.2:p.Leu1252=
ENST00000497488.2:c.2866_2868delinsCTG ENSP00000418986.2:p.Leu956=
ENST00000618469.2:c.3754_3756delinsCTG ENSP00000478114.2:p.Leu1252=
ENST00000634433.2:c.3631_3633delinsCTG ENSP00000489431.2:p.Leu1211=
ENST00000644379.2:c.3754_3756delinsCTG ENSP00000496570.2:p.Leu1252=
ENST00000644555.2:c.647-745_647-743delinsCTG ENSP00000494614.2:n.647-745_647-743delins...
ENST00000652672.2:c.3613_3615delinsCTG ENSP00000498906.2:p.Leu1205=
ENST00000484087.6:c.665-745_665-743delinsCTG ENSP00000419481.2:n.665-745_665-743delins...
ENST00000700182.1:c.707-745_707-743delinsCTG ENSP00000514849.1:n.707-745_707-743delins...
ENST00000357654.9:c.3754_3756delinsCTG MANE Select ENSP00000350283.3:p.Leu1252=
ENST00000471181.7:c.3754_3756delinsCTG ENSP00000418960.2:p.Leu1252=
ENST00000644379.1:c.75_77delinsCTG
ENST00000352993.7:c.671-745_671-743delinsCTG ENSP00000312236.5:n.671-745_671-743delins...
ENST00000354071.7:c.3754_3756delinsCTG ENSP00000326002.7:p.Leu1252=
ENST00000357654.7:c.3754_3756delinsCTG ENSP00000350283.3:p.Leu1252=
ENST00000461221.5:c.*3537_*3539delinsCTG ENSP00000418548.1:n.*3537_*3539delinsCTG
ENST00000461574.1:c.48_50delinsCTG
ENST00000468300.5:c.788-745_788-743delinsCTG ENSP00000417148.1:n.788-745_788-743delins...
ENST00000471181.6:c.3754_3756delinsCTG ENSP00000418960.2:p.Leu1252=
ENST00000478531.5:c.785-745_785-743delinsCTG ENSP00000420412.1:n.785-745_785-743delins...
ENST00000484087.5:c.410-745_410-743delinsCTG ENSP00000419481.1:n.410-745_410-743delins...
ENST00000487825.5:c.413-745_413-743delinsCTG ENSP00000418212.1:n.413-745_413-743delins...
ENST00000491747.6:c.788-745_788-743delinsCTG ENSP00000420705.2:n.788-745_788-743delins...
ENST00000493795.5:c.3613_3615delinsCTG ENSP00000418775.1:p.Leu1205=
ENST00000493919.5:c.647-745_647-743delinsCTG ENSP00000418819.1:n.647-745_647-743delins...
ENST00000586385.5:c.5-27826_5-27824delinsCTG ENSP00000465818.1:n.5-27826_5-27824delins...
ENST00000591534.5:c.-43-17256_-43-17254delinsCTG ENSP00000467329.1:n.-43-17256_-43-17254de...
ENST00000591849.5:c.-99+33494_-99+33496delinsCTG ENSP00000465347.1:n.-99+33494_-99+33496de...
NM_007294.3:c.3754_3756delinsCTG , LRG_292t1:c.3754_3756delinsCTG NP_009225.1:p.Leu1252=
NM_007297.3:c.3613_3615delinsCTG NP_009228.2:p.Leu1205=
NM_007298.3:c.788-745_788-743delinsCTG NP_009229.2:n.788-745_788-743delinsCTG
NM_007299.3:c.788-745_788-743delinsCTG NP_009230.2:n.788-745_788-743delinsCTG
NM_007300.3:c.3754_3756delinsCTG NP_009231.2:p.Leu1252=
NR_027676.1:n.3890_3892delinsCTG
NM_007294.4:c.3754_3756delinsCTG MANE Select NP_009225.1:p.Leu1252=
NM_007297.4:c.3613_3615delinsCTG NP_009228.2:p.Leu1205=
NM_007299.4:c.788-745_788-743delinsCTG NP_009230.2:n.788-745_788-743delinsCTG
NM_007300.4:c.3754_3756delinsCTG NP_009231.2:p.Leu1252=
NR_027676.2:n.3931_3933delinsCTG