Canonical Allele Identifier: CA1628833108
Gene: EFHC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.52479641G= , CM000668.2:g.52479641G= GRCh38
NC_000006.11:g.52344439G= , CM000668.1:g.52344439G= GRCh37
NC_000006.10:g.52452398G= NCBI36
NG_016760.1:g.64446G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371068.11:c.1494G= MANE Select ENSP00000360107.4:p.Val498=
ENST00000480623.6:c.1494G= ENSP00000434498.2:p.Val498=
ENST00000635760.1:c.1170G= ENSP00000489765.1:p.Val390=
ENST00000635812.1:c.*795G= ENSP00000490859.1:n.*795G=
ENST00000635866.1:c.*1363G= ENSP00000489866.1:n.*1363G=
ENST00000635911.1:n.3012G=
ENST00000635984.1:c.1170G= ENSP00000489921.1:p.Val390=
ENST00000635996.1:c.1494G= ENSP00000490256.1:p.Val498=
ENST00000636107.1:c.1494G= ENSP00000489680.1:p.Val498=
ENST00000636311.1:n.1388G=
ENST00000636343.1:c.1160G=
ENST00000636379.1:c.1206G= ENSP00000490622.1:p.Val402=
ENST00000636398.1:c.1194G= ENSP00000489654.1:n.1194G=
ENST00000636489.1:c.1437G= ENSP00000489998.1:p.Val479=
ENST00000636616.1:n.1055G=
ENST00000636702.1:c.1464G= ENSP00000489623.1:p.Val488=
ENST00000636954.1:c.1437G= ENSP00000489966.1:p.Val479=
ENST00000637089.1:c.1494G= ENSP00000489854.1:p.Val498=
ENST00000637121.1:n.1296G=
ENST00000637263.1:c.1494G= ENSP00000489700.1:p.Val498=
ENST00000637340.1:n.3419G=
ENST00000637353.1:c.1494G= ENSP00000490441.1:p.Val498=
ENST00000637602.1:c.*1195G= ENSP00000490074.1:n.*1195G=
ENST00000637849.1:n.1558G=
ENST00000637874.1:c.439G= ENSP00000490348.1:n.439G=
ENST00000637892.1:n.1698G=
ENST00000371068.9:c.1494G= ENSP00000360107.4:p.Val498=
ENST00000480623.5:c.*1914G= ENSP00000434498.1:n.*1914G=
ENST00000538167.2:c.1437G= ENSP00000444521.1:p.Val479=
NM_001172420.1:c.1437G= NP_001165891.1:p.Val479=
NM_018100.3:c.1494G= NP_060570.2:p.Val498=
NR_033327.1:n.2966G=
NM_018100.4:c.1494G= MANE Select NP_060570.2:p.Val498=
NM_001172420.2:c.1437G= NP_001165891.1:p.Val479=
NR_033327.2:n.2820G=