Canonical Allele Identifier: CA1946721049
Gene: ECHS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133373275C= , CM000672.2:g.133373275C= GRCh38
NC_000010.10:g.135186779C= , CM000672.1:g.135186779C= GRCh37
NC_000010.9:g.135036769C= NCBI36
NG_042077.1:g.5130G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368547.4:c.59G= MANE Select ENSP00000357535.3:p.Arg20=
ENST00000368547.3:c.59G= ENSP00000357535.3:p.Arg20=
NM_004092.3:c.59G= NP_004083.3:p.Arg20=
XR_002956965.1:n.122G=
NM_004092.4:c.59G= MANE Select NP_004083.3:p.Arg20=