Canonical Allele Identifier: CA1946753029
Gene: ECHS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133366153T= , CM000672.2:g.133366153T= GRCh38
NC_000010.10:g.135179657T= , CM000672.1:g.135179657T= GRCh37
NC_000010.9:g.135029647T= NCBI36
NG_042077.1:g.12252A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368547.4:c.620-58A= MANE Select ENSP00000357535.3:n.620-58A=
ENST00000368547.3:c.620-58A= ENSP00000357535.3:n.620-58A=
NM_004092.3:c.620-58A= NP_004083.3:n.620-58A=
XR_002956965.1:n.1418A=
NM_004092.4:c.620-58A= MANE Select NP_004083.3:n.620-58A=