Canonical Allele Identifier: CA209479893
Gene: CHST3 HGNC NCBI

Linked Data

dbSNP Id: rs372345396
MyVariant Identifiers: chr10:g.73769596_73769597insGG (hg19) chr10:g.72009838_72009839insGG (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.72009839_72009840insGG , CM000672.2:g.72009839_72009840insGG GRCh38
NC_000010.10:g.73769597_73769598insGG , CM000672.1:g.73769597_73769598insGG GRCh37
NC_000010.9:g.73439603_73439604insGG NCBI36
NG_012635.1:g.50478_50479insGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000373115.5:c.*1368_*1369insGG MANE Select ENSP00000362207.4:n.*1368_*1369insGG
ENST00000373115.4:c.*1368_*1369insGG ENSP00000362207.4:n.*1368_*1369insGG
NM_004273.4:c.*1368_*1369insGG NP_004264.2:n.*1368_*1369insGG
XM_006718075.2:c.*1368_*1369insGG XP_006718138.1:n.*1368_*1369insGG
XM_011540369.1:c.*1368_*1369insGG XP_011538671.1:n.*1368_*1369insGG
XM_006718075.4:c.*1368_*1369insGG XP_006718138.1:n.*1368_*1369insGG
XM_011540369.2:c.*1368_*1369insGG XP_011538671.1:n.*1368_*1369insGG
NM_004273.5:c.*1368_*1369insGG MANE Select NP_004264.2:n.*1368_*1369insGG
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