Canonical Allele Identifier: CA364456849
Gene: EFHC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.52479041C>G , CM000668.2:g.52479041C>G GRCh38
NC_000006.11:g.52343839C>G , CM000668.1:g.52343839C>G GRCh37
NC_000006.10:g.52451798C>G NCBI36
NG_016760.1:g.63846C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371068.11:c.1283C>G MANE Select ENSP00000360107.4:p.Ser428Cys
ENST00000480623.6:c.1283C>G ENSP00000434498.2:p.Ser428Cys
ENST00000635760.1:c.959C>G ENSP00000489765.1:p.Ser320Cys
ENST00000635812.1:c.*584C>G ENSP00000490859.1:n.*584C>G
ENST00000635866.1:c.*1152C>G ENSP00000489866.1:n.*1152C>G
ENST00000635911.1:n.2801C>G
ENST00000635984.1:c.959C>G ENSP00000489921.1:p.Ser320Cys
ENST00000635996.1:c.1283C>G ENSP00000490256.1:p.Ser428Cys
ENST00000636107.1:c.1283C>G ENSP00000489680.1:p.Ser428Cys
ENST00000636311.1:n.1177C>G
ENST00000636343.1:c.949C>G
ENST00000636379.1:c.995C>G ENSP00000490622.1:p.Ser332Cys
ENST00000636398.1:c.983C>G ENSP00000489654.1:n.983C>G
ENST00000636489.1:c.1226C>G ENSP00000489998.1:p.Ser409Cys
ENST00000636616.1:n.895-51C>G
ENST00000636702.1:c.1253C>G ENSP00000489623.1:p.Ser418Cys
ENST00000636954.1:c.1226C>G ENSP00000489966.1:p.Ser409Cys
ENST00000637089.1:c.1283C>G ENSP00000489854.1:p.Ser428Cys
ENST00000637121.1:n.1085C>G
ENST00000637263.1:c.1283C>G ENSP00000489700.1:p.Ser428Cys
ENST00000637340.1:n.3208C>G
ENST00000637353.1:c.1283C>G ENSP00000490441.1:p.Ser428Cys
ENST00000637602.1:c.*984C>G ENSP00000490074.1:n.*984C>G
ENST00000637849.1:n.1347C>G
ENST00000637874.1:c.228C>G ENSP00000490348.1:n.228C>G
ENST00000637892.1:n.1487C>G
ENST00000371068.9:c.1283C>G ENSP00000360107.4:p.Ser428Cys
ENST00000480623.5:c.*1703C>G ENSP00000434498.1:n.*1703C>G
ENST00000538167.2:c.1226C>G ENSP00000444521.1:p.Ser409Cys
NM_001172420.1:c.1226C>G NP_001165891.1:p.Ser409Cys
NM_018100.3:c.1283C>G NP_060570.2:p.Ser428Cys
NR_033327.1:n.2755C>G
NM_018100.4:c.1283C>G MANE Select NP_060570.2:p.Ser428Cys
NM_001172420.2:c.1226C>G NP_001165891.1:p.Ser409Cys
NR_033327.2:n.2609C>G