Canonical Allele Identifier: CA2260783854
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43093336_43093337delinsTC , CM000679.2:g.43093336_43093337delinsTC GRCh38
NC_000017.10:g.41245353_41245354delinsTC , CM000679.1:g.41245353_41245354delinsTC GRCh37
NC_000017.9:g.38498879_38498880delinsTC NCBI36
NG_005905.2:g.124647_124648delinsGA , LRG_292:g.124647_124648delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000354071.8:n.2258_2259delinsGA
ENST00000461574.2:c.2194_2195delinsGA ENSP00000417241.2:p.Glu732=
ENST00000470026.6:c.2194_2195delinsGA ENSP00000419274.2:p.Glu732=
ENST00000473961.6:c.2068_2069delinsGA ENSP00000420201.2:p.Glu690=
ENST00000476777.6:c.2191_2192delinsGA ENSP00000417554.2:p.Glu731=
ENST00000477152.6:c.2116_2117delinsGA ENSP00000419988.2:p.Glu706=
ENST00000478531.6:c.784+1407_784+1408delinsGA ENSP00000420412.2:n.784+1407_784+1408delinsGA
ENST00000489037.2:c.2116_2117delinsGA ENSP00000420781.2:p.Glu706=
ENST00000493919.6:c.646+1407_646+1408delinsGA ENSP00000418819.2:n.646+1407_646+1408delinsGA
ENST00000494123.6:c.2194_2195delinsGA ENSP00000419103.2:p.Glu732=
ENST00000497488.2:c.1306_1307delinsGA ENSP00000418986.2:p.Glu436=
ENST00000618469.2:c.2194_2195delinsGA ENSP00000478114.2:p.Glu732=
ENST00000634433.2:c.2071_2072delinsGA ENSP00000489431.2:p.Glu691=
ENST00000644379.2:c.2194_2195delinsGA ENSP00000496570.2:p.Glu732=
ENST00000644555.2:c.646+1407_646+1408delinsGA ENSP00000494614.2:n.646+1407_646+1408delinsGA
ENST00000652672.2:c.2053_2054delinsGA ENSP00000498906.2:p.Glu685=
ENST00000484087.6:c.664+1407_664+1408delinsGA ENSP00000419481.2:n.664+1407_664+1408delinsGA
ENST00000700182.1:c.706+1407_706+1408delinsGA ENSP00000514849.1:n.706+1407_706+1408delinsGA
ENST00000357654.9:c.2194_2195delinsGA MANE Select ENSP00000350283.3:p.Glu732=
ENST00000471181.7:c.2194_2195delinsGA ENSP00000418960.2:p.Glu732=
ENST00000352993.7:c.671-2305_671-2304delinsGA ENSP00000312236.5:n.671-2305_671-2304delinsGA
ENST00000354071.7:c.2194_2195delinsGA ENSP00000326002.7:p.Glu732=
ENST00000357654.7:c.2194_2195delinsGA ENSP00000350283.3:p.Glu732=
ENST00000461221.5:c.*1977_*1978delinsGA ENSP00000418548.1:n.*1977_*1978delinsGA
ENST00000468300.5:c.787+1407_787+1408delinsGA ENSP00000417148.1:n.787+1407_787+1408delinsGA
ENST00000471181.6:c.2194_2195delinsGA ENSP00000418960.2:p.Glu732=
ENST00000478531.5:c.784+1407_784+1408delinsGA ENSP00000420412.1:n.784+1407_784+1408delinsGA
ENST00000484087.5:c.409+1407_409+1408delinsGA ENSP00000419481.1:n.409+1407_409+1408delinsGA
ENST00000487825.5:c.412+1407_412+1408delinsGA ENSP00000418212.1:n.412+1407_412+1408delinsGA
ENST00000491747.6:c.787+1407_787+1408delinsGA ENSP00000420705.2:n.787+1407_787+1408delinsGA
ENST00000493795.5:c.2053_2054delinsGA ENSP00000418775.1:p.Glu685=
ENST00000493919.5:c.646+1407_646+1408delinsGA ENSP00000418819.1:n.646+1407_646+1408delinsGA
ENST00000586385.5:c.5-29386_5-29385delinsGA ENSP00000465818.1:n.5-29386_5-29385delinsGA
ENST00000591534.5:c.-43-18816_-43-18815delinsGA ENSP00000467329.1:n.-43-18816_-43-18815delinsGA
ENST00000591849.5:c.-99+31934_-99+31935delinsGA ENSP00000465347.1:n.-99+31934_-99+31935delinsGA
ENST00000634433.1:c.2071_2072delinsGA ENSP00000489431.1:p.Glu691=
NM_007294.3:c.2194_2195delinsGA , LRG_292t1:c.2194_2195delinsGA NP_009225.1:p.Glu732=
NM_007297.3:c.2053_2054delinsGA NP_009228.2:p.Glu685=
NM_007298.3:c.787+1407_787+1408delinsGA NP_009229.2:n.787+1407_787+1408delinsGA
NM_007299.3:c.787+1407_787+1408delinsGA NP_009230.2:n.787+1407_787+1408delinsGA
NM_007300.3:c.2194_2195delinsGA NP_009231.2:p.Glu732=
NR_027676.1:n.2330_2331delinsGA
NM_007294.4:c.2194_2195delinsGA MANE Select NP_009225.1:p.Glu732=
NM_007297.4:c.2053_2054delinsGA NP_009228.2:p.Glu685=
NM_007299.4:c.787+1407_787+1408delinsGA NP_009230.2:n.787+1407_787+1408delinsGA
NM_007300.4:c.2194_2195delinsGA NP_009231.2:p.Glu732=
NR_027676.2:n.2371_2372delinsGA