Canonical Allele Identifier: CA2611598645
Gene: ECHS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133373354dup , CM000672.2:g.133373354dup GRCh38
NC_000010.10:g.135186858dup , CM000672.1:g.135186858dup GRCh37
NC_000010.9:g.135036848dup NCBI36
NG_042077.1:g.5053dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000368547.4:c.-19dup MANE Select ENSP00000357535.3:n.-19dup
ENST00000368547.3:c.-19dup ENSP00000357535.3:n.-19dup
NM_004092.3:c.-19dup NP_004083.3:n.-19dup
XR_002956965.1:n.45dup
NM_004092.4:c.-19dup MANE Select NP_004083.3:n.-19dup