Canonical Allele Identifier: CA2611598617
Gene: ECHS1 HGNC NCBI

Linked Data

gnomAD v4: 10-133373291-GC-G
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.133373292del , CM000672.2:g.133373292del GRCh38
NC_000010.10:g.135186796del , CM000672.1:g.135186796del GRCh37
NC_000010.9:g.135036786del NCBI36
NG_042077.1:g.5113del

Transcript Alleles

HGVS Amino-acid Change
ENST00000368547.4:c.42del MANE Select ENSP00000357535.3:p.Leu15Ter
ENST00000368547.3:c.42del ENSP00000357535.3:p.Leu15Ter
NM_004092.3:c.42del NP_004083.3:p.Leu15Ter
XR_002956965.1:n.105del
NM_004092.4:c.42del MANE Select NP_004083.3:p.Leu15Ter
Search 100 bp 5'
Search 100 bp 3'