Canonical Allele Identifier: CA1946721055
Gene: ECHS1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133373285G= , CM000672.2:g.133373285G= GRCh38
NC_000010.10:g.135186789G= , CM000672.1:g.135186789G= GRCh37
NC_000010.9:g.135036779G= NCBI36
NG_042077.1:g.5120C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368547.4:c.49C= MANE Select ENSP00000357535.3:p.Pro17=
ENST00000368547.3:c.49C= ENSP00000357535.3:p.Pro17=
NM_004092.3:c.49C= NP_004083.3:p.Pro17=
XR_002956965.1:n.112C=
NM_004092.4:c.49C= MANE Select NP_004083.3:p.Pro17=
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