Canonical Allele Identifier: CA364458134
Gene: EFHC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.52479718C>A , CM000668.2:g.52479718C>A GRCh38
NC_000006.11:g.52344516C>A , CM000668.1:g.52344516C>A GRCh37
NC_000006.10:g.52452475C>A NCBI36
NG_016760.1:g.64523C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371068.11:c.1571C>A MANE Select ENSP00000360107.4:p.Ser524Ter
ENST00000480623.6:c.1571C>A ENSP00000434498.2:p.Ser524Ter
ENST00000635760.1:c.1247C>A ENSP00000489765.1:p.Ser416Ter
ENST00000635812.1:c.*872C>A ENSP00000490859.1:n.*872C>A
ENST00000635866.1:c.*1440C>A ENSP00000489866.1:n.*1440C>A
ENST00000635911.1:n.3089C>A
ENST00000635984.1:c.1247C>A ENSP00000489921.1:p.Ser416Ter
ENST00000635996.1:c.1571C>A ENSP00000490256.1:p.Ser524Ter
ENST00000636107.1:c.1571C>A ENSP00000489680.1:p.Ser524Ter
ENST00000636311.1:n.1465C>A
ENST00000636343.1:c.1237C>A
ENST00000636379.1:c.1283C>A ENSP00000490622.1:p.Ser428Ter
ENST00000636398.1:c.1271C>A ENSP00000489654.1:n.1271C>A
ENST00000636489.1:c.1514C>A ENSP00000489998.1:p.Ser505Ter
ENST00000636616.1:n.1132C>A
ENST00000636702.1:c.1541C>A ENSP00000489623.1:p.Ser514Ter
ENST00000636954.1:c.1514C>A ENSP00000489966.1:p.Ser505Ter
ENST00000637089.1:c.1571C>A ENSP00000489854.1:p.Ser524Ter
ENST00000637121.1:n.1373C>A
ENST00000637263.1:c.1571C>A ENSP00000489700.1:p.Ser524Ter
ENST00000637340.1:n.3496C>A
ENST00000637353.1:c.1571C>A ENSP00000490441.1:p.Ser524Ter
ENST00000637602.1:c.*1272C>A ENSP00000490074.1:n.*1272C>A
ENST00000637849.1:n.1635C>A
ENST00000637892.1:n.1775C>A
ENST00000371068.9:c.1571C>A ENSP00000360107.4:p.Ser524Ter
ENST00000480623.5:c.*1991C>A ENSP00000434498.1:n.*1991C>A
ENST00000538167.2:c.1514C>A ENSP00000444521.1:p.Ser505Ter
NM_001172420.1:c.1514C>A NP_001165891.1:p.Ser505Ter
NM_018100.3:c.1571C>A NP_060570.2:p.Ser524Ter
NR_033327.1:n.3043C>A
NM_018100.4:c.1571C>A MANE Select NP_060570.2:p.Ser524Ter
NM_001172420.2:c.1514C>A NP_001165891.1:p.Ser505Ter
NR_033327.2:n.2897C>A