Canonical Allele Identifier: CA1946753062
Gene: ECHS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133366188A= , CM000672.2:g.133366188A= GRCh38
NC_000010.10:g.135179692A= , CM000672.1:g.135179692A= GRCh37
NC_000010.9:g.135029682A= NCBI36
NG_042077.1:g.12217T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368547.4:c.620-93T= MANE Select ENSP00000357535.3:n.620-93T=
ENST00000368547.3:c.620-93T= ENSP00000357535.3:n.620-93T=
NM_004092.3:c.620-93T= NP_004083.3:n.620-93T=
XR_002956965.1:n.1383T=
NM_004092.4:c.620-93T= MANE Select NP_004083.3:n.620-93T=