Canonical Allele Identifier: CA2611597167
Gene: ECHS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133366151del , CM000672.2:g.133366151del GRCh38
NC_000010.10:g.135179655del , CM000672.1:g.135179655del GRCh37
NC_000010.9:g.135029645del NCBI36
NG_042077.1:g.12255del

Transcript Alleles

HGVS Amino-acid Change
ENST00000368547.4:c.620-55del MANE Select ENSP00000357535.3:n.620-55del
ENST00000368547.3:c.620-55del ENSP00000357535.3:n.620-55del
NM_004092.3:c.620-55del NP_004083.3:n.620-55del
XR_002956965.1:n.1421del
NM_004092.4:c.620-55del MANE Select NP_004083.3:n.620-55del