Canonical Allele Identifier: CA364451985
Gene: EFHC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.52452702C>G , CM000668.2:g.52452702C>G GRCh38
NC_000006.11:g.52317500C>G , CM000668.1:g.52317500C>G GRCh37
NC_000006.10:g.52425459C>G NCBI36
NG_016760.1:g.37507C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371068.11:c.588C>G MANE Select ENSP00000360107.4:p.Ser196Arg
ENST00000480623.6:c.588C>G ENSP00000434498.2:p.Ser196Arg
ENST00000635760.1:c.264C>G ENSP00000489765.1:p.Ser88Arg
ENST00000635812.1:c.588C>G ENSP00000490859.1:p.Ser196Arg
ENST00000635866.1:c.*457C>G ENSP00000489866.1:n.*457C>G
ENST00000635911.1:n.849C>G
ENST00000635984.1:c.264C>G ENSP00000489921.1:p.Ser88Arg
ENST00000635996.1:c.588C>G ENSP00000490256.1:p.Ser196Arg
ENST00000636107.1:c.588C>G ENSP00000489680.1:p.Ser196Arg
ENST00000636253.1:n.242C>G
ENST00000636311.1:n.482C>G
ENST00000636343.1:c.254C>G
ENST00000636379.1:c.300C>G ENSP00000490622.1:p.Ser100Arg
ENST00000636398.1:c.255C>G ENSP00000489654.1:p.Ser85Arg
ENST00000636489.1:c.531C>G ENSP00000489998.1:p.Ser177Arg
ENST00000636702.1:c.558C>G ENSP00000489623.1:p.Ser186Arg
ENST00000636954.1:c.531C>G ENSP00000489966.1:p.Ser177Arg
ENST00000637089.1:c.588C>G ENSP00000489854.1:p.Ser196Arg
ENST00000637200.1:c.*604C>G ENSP00000490567.1:n.*604C>G
ENST00000637263.1:c.588C>G ENSP00000489700.1:p.Ser196Arg
ENST00000637340.1:n.1256C>G
ENST00000637353.1:c.588C>G ENSP00000490441.1:p.Ser196Arg
ENST00000637602.1:c.*289C>G ENSP00000490074.1:n.*289C>G
ENST00000637849.1:n.652C>G
ENST00000637892.1:n.792C>G
ENST00000638075.1:c.-31C>G ENSP00000490711.1:n.-31C>G
ENST00000371068.9:c.588C>G ENSP00000360107.4:p.Ser196Arg
ENST00000480623.5:c.588C>G ENSP00000434498.1:p.Ser196Arg
ENST00000538167.2:c.531C>G ENSP00000444521.1:p.Ser177Arg
NM_001172420.1:c.531C>G NP_001165891.1:p.Ser177Arg
NM_018100.3:c.588C>G NP_060570.2:p.Ser196Arg
NR_033327.1:n.803C>G
NM_018100.4:c.588C>G MANE Select NP_060570.2:p.Ser196Arg
NM_001172420.2:c.531C>G NP_001165891.1:p.Ser177Arg
NR_033327.2:n.657C>G