Canonical Allele Identifier: CA2627825034
Gene: CHST14 HGNC NCBI

Linked Data

gnomAD v4: 15-40472383-CA-C
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40472385del , CM000677.2:g.40472385del GRCh38
NC_000015.9:g.40764584del , CM000677.1:g.40764584del GRCh37
NC_000015.8:g.38551876del NCBI36
NG_017074.1:g.6425del , LRG_600:g.6425del

Transcript Alleles

HGVS Amino-acid Change
ENST00000306243.7:c.*41del MANE Select ENSP00000307297.6:n.*41del
ENST00000306243.6:c.*41del ENSP00000307297.5:n.*41del
ENST00000559991.1:c.*41del ENSP00000453882.1:n.*41del
NM_130468.3:c.*41del , LRG_600t1:c.*41del NP_569735.1:n.*41del
NM_130468.4:c.*41del MANE Select NP_569735.1:n.*41del
Search 100 bp 5'
Search 100 bp 3'