Canonical Allele Identifier: CA1628833321
Gene: EFHC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.52479740T= , CM000668.2:g.52479740T= GRCh38
NC_000006.11:g.52344538T= , CM000668.1:g.52344538T= GRCh37
NC_000006.10:g.52452497T= NCBI36
NG_016760.1:g.64545T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371068.11:c.1593T= MANE Select ENSP00000360107.4:p.Ile531=
ENST00000480623.6:c.1593T= ENSP00000434498.2:p.Ile531=
ENST00000635760.1:c.1269T= ENSP00000489765.1:p.Ile423=
ENST00000635812.1:c.*894T= ENSP00000490859.1:n.*894T=
ENST00000635866.1:c.*1462T= ENSP00000489866.1:n.*1462T=
ENST00000635911.1:n.3111T=
ENST00000635984.1:c.1269T= ENSP00000489921.1:p.Ile423=
ENST00000635996.1:c.1593T= ENSP00000490256.1:p.Ile531=
ENST00000636107.1:c.1593T= ENSP00000489680.1:p.Ile531=
ENST00000636311.1:n.1487T=
ENST00000636343.1:c.1259T=
ENST00000636379.1:c.1305T= ENSP00000490622.1:p.Ile435=
ENST00000636398.1:c.1293T= ENSP00000489654.1:n.1293T=
ENST00000636489.1:c.1536T= ENSP00000489998.1:p.Ile512=
ENST00000636616.1:n.1154T=
ENST00000636702.1:c.1563T= ENSP00000489623.1:p.Ile521=
ENST00000636954.1:c.1536T= ENSP00000489966.1:p.Ile512=
ENST00000637089.1:c.1593T= ENSP00000489854.1:p.Ile531=
ENST00000637121.1:n.1395T=
ENST00000637263.1:c.1593T= ENSP00000489700.1:p.Ile531=
ENST00000637340.1:n.3518T=
ENST00000637353.1:c.1593T= ENSP00000490441.1:p.Ile531=
ENST00000637602.1:c.*1294T= ENSP00000490074.1:n.*1294T=
ENST00000637849.1:n.1657T=
ENST00000637892.1:n.1797T=
ENST00000371068.9:c.1593T= ENSP00000360107.4:p.Ile531=
ENST00000480623.5:c.*2013T= ENSP00000434498.1:n.*2013T=
ENST00000538167.2:c.1536T= ENSP00000444521.1:p.Ile512=
NM_001172420.1:c.1536T= NP_001165891.1:p.Ile512=
NM_018100.3:c.1593T= NP_060570.2:p.Ile531=
NR_033327.1:n.3065T=
NM_018100.4:c.1593T= MANE Select NP_060570.2:p.Ile531=
NM_001172420.2:c.1536T= NP_001165891.1:p.Ile512=
NR_033327.2:n.2919T=