Canonical Allele Identifier: CA378819422
Gene: ECHS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.135179576C>A (hg19) chr10:g.133366072C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133366072C>A , CM000672.2:g.133366072C>A GRCh38
NC_000010.10:g.135179576C>A , CM000672.1:g.135179576C>A GRCh37
NC_000010.9:g.135029566C>A NCBI36
NG_042077.1:g.12333G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000368547.4:c.643G>T MANE Select ENSP00000357535.3:p.Val215Phe
ENST00000368547.3:c.643G>T ENSP00000357535.3:p.Val215Phe
NM_004092.3:c.643G>T NP_004083.3:p.Val215Phe
XR_002956965.1:n.1499G>T
NM_004092.4:c.643G>T MANE Select NP_004083.3:p.Val215Phe
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