Canonical Allele Identifier: CA1946752995
Gene: ECHS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133366112T= , CM000672.2:g.133366112T= GRCh38
NC_000010.10:g.135179616T= , CM000672.1:g.135179616T= GRCh37
NC_000010.9:g.135029606T= NCBI36
NG_042077.1:g.12293A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368547.4:c.620-17A= MANE Select ENSP00000357535.3:n.620-17A=
ENST00000368547.3:c.620-17A= ENSP00000357535.3:n.620-17A=
NM_004092.3:c.620-17A= NP_004083.3:n.620-17A=
XR_002956965.1:n.1459A=
NM_004092.4:c.620-17A= MANE Select NP_004083.3:n.620-17A=