Canonical Allele Identifier: CA364458240
Gene: EFHC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.52479772C>A , CM000668.2:g.52479772C>A GRCh38
NC_000006.11:g.52344570C>A , CM000668.1:g.52344570C>A GRCh37
NC_000006.10:g.52452529C>A NCBI36
NG_016760.1:g.64577C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371068.11:c.1625C>A MANE Select ENSP00000360107.4:p.Ala542Asp
ENST00000480623.6:c.1625C>A ENSP00000434498.2:p.Ala542Asp
ENST00000635760.1:c.1301C>A ENSP00000489765.1:p.Ala434Asp
ENST00000635812.1:c.*926C>A ENSP00000490859.1:n.*926C>A
ENST00000635866.1:c.*1494C>A ENSP00000489866.1:n.*1494C>A
ENST00000635911.1:n.3143C>A
ENST00000635984.1:c.1301C>A ENSP00000489921.1:p.Ala434Asp
ENST00000635996.1:c.1625C>A ENSP00000490256.1:p.Ala542Asp
ENST00000636107.1:c.1625C>A ENSP00000489680.1:p.Ala542Asp
ENST00000636311.1:n.1519C>A
ENST00000636343.1:c.1291C>A
ENST00000636379.1:c.1337C>A ENSP00000490622.1:p.Ala446Asp
ENST00000636398.1:c.1325C>A ENSP00000489654.1:n.1325C>A
ENST00000636489.1:c.1568C>A ENSP00000489998.1:p.Ala523Asp
ENST00000636616.1:n.1186C>A
ENST00000636702.1:c.1595C>A ENSP00000489623.1:p.Ala532Asp
ENST00000636954.1:c.1568C>A ENSP00000489966.1:p.Ala523Asp
ENST00000637089.1:c.1625C>A ENSP00000489854.1:p.Ala542Asp
ENST00000637121.1:n.1427C>A
ENST00000637263.1:c.1625C>A ENSP00000489700.1:p.Ala542Asp
ENST00000637340.1:n.3550C>A
ENST00000637353.1:c.1625C>A ENSP00000490441.1:p.Ala542Asp
ENST00000637602.1:c.*1326C>A ENSP00000490074.1:n.*1326C>A
ENST00000637849.1:n.1689C>A
ENST00000637892.1:n.1829C>A
ENST00000371068.9:c.1625C>A ENSP00000360107.4:p.Ala542Asp
ENST00000480623.5:c.*2045C>A ENSP00000434498.1:n.*2045C>A
ENST00000538167.2:c.1568C>A ENSP00000444521.1:p.Ala523Asp
NM_001172420.1:c.1568C>A NP_001165891.1:p.Ala523Asp
NM_018100.3:c.1625C>A NP_060570.2:p.Ala542Asp
NR_033327.1:n.3097C>A
NM_018100.4:c.1625C>A MANE Select NP_060570.2:p.Ala542Asp
NM_001172420.2:c.1568C>A NP_001165891.1:p.Ala523Asp
NR_033327.2:n.2951C>A