Canonical Allele Identifier: CA1628833361
Gene: EFHC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.52479758G= , CM000668.2:g.52479758G= GRCh38
NC_000006.11:g.52344556G= , CM000668.1:g.52344556G= GRCh37
NC_000006.10:g.52452515G= NCBI36
NG_016760.1:g.64563G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371068.11:c.1611G= MANE Select ENSP00000360107.4:p.Lys537=
ENST00000480623.6:c.1611G= ENSP00000434498.2:p.Lys537=
ENST00000635760.1:c.1287G= ENSP00000489765.1:p.Lys429=
ENST00000635812.1:c.*912G= ENSP00000490859.1:n.*912G=
ENST00000635866.1:c.*1480G= ENSP00000489866.1:n.*1480G=
ENST00000635911.1:n.3129G=
ENST00000635984.1:c.1287G= ENSP00000489921.1:p.Lys429=
ENST00000635996.1:c.1611G= ENSP00000490256.1:p.Lys537=
ENST00000636107.1:c.1611G= ENSP00000489680.1:p.Lys537=
ENST00000636311.1:n.1505G=
ENST00000636343.1:c.1277G=
ENST00000636379.1:c.1323G= ENSP00000490622.1:p.Lys441=
ENST00000636398.1:c.1311G= ENSP00000489654.1:n.1311G=
ENST00000636489.1:c.1554G= ENSP00000489998.1:p.Lys518=
ENST00000636616.1:n.1172G=
ENST00000636702.1:c.1581G= ENSP00000489623.1:p.Lys527=
ENST00000636954.1:c.1554G= ENSP00000489966.1:p.Lys518=
ENST00000637089.1:c.1611G= ENSP00000489854.1:p.Lys537=
ENST00000637121.1:n.1413G=
ENST00000637263.1:c.1611G= ENSP00000489700.1:p.Lys537=
ENST00000637340.1:n.3536G=
ENST00000637353.1:c.1611G= ENSP00000490441.1:p.Lys537=
ENST00000637602.1:c.*1312G= ENSP00000490074.1:n.*1312G=
ENST00000637849.1:n.1675G=
ENST00000637892.1:n.1815G=
ENST00000371068.9:c.1611G= ENSP00000360107.4:p.Lys537=
ENST00000480623.5:c.*2031G= ENSP00000434498.1:n.*2031G=
ENST00000538167.2:c.1554G= ENSP00000444521.1:p.Lys518=
NM_001172420.1:c.1554G= NP_001165891.1:p.Lys518=
NM_018100.3:c.1611G= NP_060570.2:p.Lys537=
NR_033327.1:n.3083G=
NM_018100.4:c.1611G= MANE Select NP_060570.2:p.Lys537=
NM_001172420.2:c.1554G= NP_001165891.1:p.Lys518=
NR_033327.2:n.2937G=