Canonical Allele Identifier: CA209479964
Gene: CHST3 HGNC NCBI

Linked Data

dbSNP Id: rs766100098
gnomAD v4: 10-72009999-CGT-C
MyVariant Identifiers: chr10:g.73769758_73769759del (hg19) chr10:g.72010000_72010001del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.72010001_72010002del , CM000672.2:g.72010001_72010002del GRCh38
NC_000010.10:g.73769759_73769760del , CM000672.1:g.73769759_73769760del GRCh37
NC_000010.9:g.73439765_73439766del NCBI36
NG_012635.1:g.50640_50641del

Transcript Alleles

HGVS Amino-acid Change
ENST00000373115.5:c.*1530_*1531del MANE Select ENSP00000362207.4:n.*1530_*1531del
ENST00000373115.4:c.*1530_*1531del ENSP00000362207.4:n.*1530_*1531del
NM_004273.4:c.*1530_*1531del NP_004264.2:n.*1530_*1531del
XM_006718075.2:c.*1530_*1531del XP_006718138.1:n.*1530_*1531del
XM_011540369.1:c.*1530_*1531del XP_011538671.1:n.*1530_*1531del
XM_006718075.4:c.*1530_*1531del XP_006718138.1:n.*1530_*1531del
XM_011540369.2:c.*1530_*1531del XP_011538671.1:n.*1530_*1531del
NM_004273.5:c.*1530_*1531del MANE Select NP_004264.2:n.*1530_*1531del
Search 100 bp 5'
Search 100 bp 3'