Canonical Allele Identifier: CA2609587809
Gene: CHST3 HGNC NCBI

Linked Data

gnomAD v4: 10-72009800-CT-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.72009804del , CM000672.2:g.72009804del GRCh38
NC_000010.10:g.73769562del , CM000672.1:g.73769562del GRCh37
NC_000010.9:g.73439568del NCBI36
NG_012635.1:g.50443del

Transcript Alleles

HGVS Amino-acid Change
ENST00000373115.5:c.*1333del MANE Select ENSP00000362207.4:n.*1333del
ENST00000373115.4:c.*1333del ENSP00000362207.4:n.*1333del
NM_004273.4:c.*1333del NP_004264.2:n.*1333del
XM_006718075.2:c.*1333del XP_006718138.1:n.*1333del
XM_011540369.1:c.*1333del XP_011538671.1:n.*1333del
XM_006718075.4:c.*1333del XP_006718138.1:n.*1333del
XM_011540369.2:c.*1333del XP_011538671.1:n.*1333del
NM_004273.5:c.*1333del MANE Select NP_004264.2:n.*1333del
Search 100 bp 5'
Search 100 bp 3'