Canonical Allele Identifier: CA364458242
Gene: EFHC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.52479774C>A , CM000668.2:g.52479774C>A GRCh38
NC_000006.11:g.52344572C>A , CM000668.1:g.52344572C>A GRCh37
NC_000006.10:g.52452531C>A NCBI36
NG_016760.1:g.64579C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371068.11:c.1627C>A MANE Select ENSP00000360107.4:p.Pro543Thr
ENST00000480623.6:c.1627C>A ENSP00000434498.2:p.Pro543Thr
ENST00000635760.1:c.1303C>A ENSP00000489765.1:p.Pro435Thr
ENST00000635812.1:c.*928C>A ENSP00000490859.1:n.*928C>A
ENST00000635866.1:c.*1496C>A ENSP00000489866.1:n.*1496C>A
ENST00000635911.1:n.3145C>A
ENST00000635984.1:c.1303C>A ENSP00000489921.1:p.Pro435Thr
ENST00000635996.1:c.1627C>A ENSP00000490256.1:p.Pro543Thr
ENST00000636107.1:c.1627C>A ENSP00000489680.1:p.Pro543Thr
ENST00000636311.1:n.1521C>A
ENST00000636343.1:c.1293C>A
ENST00000636379.1:c.1339C>A ENSP00000490622.1:p.Pro447Thr
ENST00000636398.1:c.1327C>A ENSP00000489654.1:n.1327C>A
ENST00000636489.1:c.1570C>A ENSP00000489998.1:p.Pro524Thr
ENST00000636616.1:n.1188C>A
ENST00000636702.1:c.1597C>A ENSP00000489623.1:p.Pro533Thr
ENST00000636954.1:c.1570C>A ENSP00000489966.1:p.Pro524Thr
ENST00000637089.1:c.1627C>A ENSP00000489854.1:p.Pro543Thr
ENST00000637121.1:n.1429C>A
ENST00000637263.1:c.1627C>A ENSP00000489700.1:p.Pro543Thr
ENST00000637340.1:n.3552C>A
ENST00000637353.1:c.1627C>A ENSP00000490441.1:p.Pro543Thr
ENST00000637602.1:c.*1328C>A ENSP00000490074.1:n.*1328C>A
ENST00000637849.1:n.1691C>A
ENST00000637892.1:n.1831C>A
ENST00000371068.9:c.1627C>A ENSP00000360107.4:p.Pro543Thr
ENST00000480623.5:c.*2047C>A ENSP00000434498.1:n.*2047C>A
ENST00000538167.2:c.1570C>A ENSP00000444521.1:p.Pro524Thr
NM_001172420.1:c.1570C>A NP_001165891.1:p.Pro524Thr
NM_018100.3:c.1627C>A NP_060570.2:p.Pro543Thr
NR_033327.1:n.3099C>A
NM_018100.4:c.1627C>A MANE Select NP_060570.2:p.Pro543Thr
NM_001172420.2:c.1570C>A NP_001165891.1:p.Pro524Thr
NR_033327.2:n.2953C>A