Canonical Allele Identifier: CA1946752775
Gene: ECHS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133365852C= , CM000672.2:g.133365852C= GRCh38
NC_000010.10:g.135179356C= , CM000672.1:g.135179356C= GRCh37
NC_000010.9:g.135029346C= NCBI36
NG_042077.1:g.12553G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368547.4:c.739+124G= MANE Select ENSP00000357535.3:n.739+124G=
ENST00000368547.3:c.739+124G= ENSP00000357535.3:n.739+124G=
NM_004092.3:c.739+124G= NP_004083.3:n.739+124G=
XR_002956965.1:n.1595+124G=
NM_004092.4:c.739+124G= MANE Select NP_004083.3:n.739+124G=