Canonical Allele Identifier: CA1946721042
Gene: ECHS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133373265G= , CM000672.2:g.133373265G= GRCh38
NC_000010.10:g.135186769G= , CM000672.1:g.135186769G= GRCh37
NC_000010.9:g.135036759G= NCBI36
NG_042077.1:g.5140C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368547.4:c.69C= MANE Select ENSP00000357535.3:p.Ala23=
ENST00000368547.3:c.69C= ENSP00000357535.3:p.Ala23=
NM_004092.3:c.69C= NP_004083.3:p.Ala23=
XR_002956965.1:n.132C=
NM_004092.4:c.69C= MANE Select NP_004083.3:p.Ala23=