Canonical Allele Identifier: CA209479899
Gene: CHST3 HGNC NCBI

Linked Data

dbSNP Id: rs535090592
gnomAD v2: 10-73769614-T-TC
gnomAD v3: 10-72009856-T-TC
gnomAD v4: 10-72009856-T-TC
MyVariant Identifiers: chr10:g.73769614_73769615insC (hg19) chr10:g.72009856_72009857insC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.72009857dup , CM000672.2:g.72009857dup GRCh38
NC_000010.10:g.73769615dup , CM000672.1:g.73769615dup GRCh37
NC_000010.9:g.73439621dup NCBI36
NG_012635.1:g.50496dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000373115.5:c.*1386dup MANE Select ENSP00000362207.4:n.*1386dup
ENST00000373115.4:c.*1386dup ENSP00000362207.4:n.*1386dup
NM_004273.4:c.*1386dup NP_004264.2:n.*1386dup
XM_006718075.2:c.*1386dup XP_006718138.1:n.*1386dup
XM_011540369.1:c.*1386dup XP_011538671.1:n.*1386dup
XM_006718075.4:c.*1386dup XP_006718138.1:n.*1386dup
XM_011540369.2:c.*1386dup XP_011538671.1:n.*1386dup
NM_004273.5:c.*1386dup MANE Select NP_004264.2:n.*1386dup
Search 100 bp 5'
Search 100 bp 3'