Canonical Allele Identifier: CA472218108
Gene: ECHS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.135179496T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133365992T>C , CM000672.2:g.133365992T>C GRCh38
NC_000010.10:g.135179496T>C , CM000672.1:g.135179496T>C GRCh37
NC_000010.9:g.135029486T>C NCBI36
NG_042077.1:g.12413A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000368547.4:c.723A>G MANE Select ENSP00000357535.3:p.Lys241=
ENST00000368547.3:c.723A>G ENSP00000357535.3:p.Lys241=
NM_004092.3:c.723A>G NP_004083.3:p.Lys241=
XR_002956965.1:n.1579A>G
NM_004092.4:c.723A>G MANE Select NP_004083.3:p.Lys241=
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