Canonical Allele Identifier: CA1946753082
Gene: ECHS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133366206C= , CM000672.2:g.133366206C= GRCh38
NC_000010.10:g.135179710C= , CM000672.1:g.135179710C= GRCh37
NC_000010.9:g.135029700C= NCBI36
NG_042077.1:g.12199G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368547.4:c.620-111G= MANE Select ENSP00000357535.3:n.620-111G=
ENST00000368547.3:c.620-111G= ENSP00000357535.3:n.620-111G=
NM_004092.3:c.620-111G= NP_004083.3:n.620-111G=
XR_002956965.1:n.1365G=
NM_004092.4:c.620-111G= MANE Select NP_004083.3:n.620-111G=