Canonical Allele Identifier: CA378824438
Gene: ECHS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133373260C>T , CM000672.2:g.133373260C>T GRCh38
NC_000010.10:g.135186764C>T , CM000672.1:g.135186764C>T GRCh37
NC_000010.9:g.135036754C>T NCBI36
NG_042077.1:g.5145G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368547.4:c.74G>A MANE Select ENSP00000357535.3:p.Arg25His
ENST00000368547.3:c.74G>A ENSP00000357535.3:p.Arg25His
NM_004092.3:c.74G>A NP_004083.3:p.Arg25His
XR_002956965.1:n.137G>A
NM_004092.4:c.74G>A MANE Select NP_004083.3:p.Arg25His