Canonical Allele Identifier: CA1946753054
Gene: ECHS1 HGNC NCBI

Linked Data

dbSNP Id: rs1849026694

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133366181dup , CM000672.2:g.133366181dup GRCh38
NC_000010.10:g.135179685dup , CM000672.1:g.135179685dup GRCh37
NC_000010.9:g.135029675dup NCBI36
NG_042077.1:g.12224dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000368547.4:c.620-86dup MANE Select ENSP00000357535.3:n.620-86dup
ENST00000368547.3:c.620-86dup ENSP00000357535.3:n.620-86dup
NM_004092.3:c.620-86dup NP_004083.3:n.620-86dup
XR_002956965.1:n.1390dup
NM_004092.4:c.620-86dup MANE Select NP_004083.3:n.620-86dup