Canonical Allele Identifier: CA2627825148
Gene: CHST14 HGNC NCBI

Linked Data

gnomAD v4: 15-40472503-AC-A
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40472506del , CM000677.2:g.40472506del GRCh38
NC_000015.9:g.40764705del , CM000677.1:g.40764705del GRCh37
NC_000015.8:g.38551997del NCBI36
NG_017074.1:g.6546del , LRG_600:g.6546del

Transcript Alleles

HGVS Amino-acid Change
ENST00000306243.7:c.*162del MANE Select ENSP00000307297.6:n.*162del
ENST00000306243.6:c.*162del ENSP00000307297.5:n.*162del
ENST00000559991.1:c.*162del ENSP00000453882.1:n.*162del
NM_130468.3:c.*162del , LRG_600t1:c.*162del NP_569735.1:n.*162del
NM_130468.4:c.*162del MANE Select NP_569735.1:n.*162del
Search 100 bp 5'
Search 100 bp 3'