Canonical Allele Identifier: CA2609588124
Gene: CHST3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.72009952_72009953insACAGG , CM000672.2:g.72009952_72009953insACAGG GRCh38
NC_000010.10:g.73769710_73769711insACAGG , CM000672.1:g.73769710_73769711insACAGG GRCh37
NC_000010.9:g.73439716_73439717insACAGG NCBI36
NG_012635.1:g.50591_50592insACAGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000373115.5:c.*1481_*1482insACAGG MANE Select ENSP00000362207.4:n.*1481_*1482insACAGG
ENST00000373115.4:c.*1481_*1482insACAGG ENSP00000362207.4:n.*1481_*1482insACAGG
NM_004273.4:c.*1481_*1482insACAGG NP_004264.2:n.*1481_*1482insACAGG
XM_006718075.2:c.*1481_*1482insACAGG XP_006718138.1:n.*1481_*1482insACAGG
XM_011540369.1:c.*1481_*1482insACAGG XP_011538671.1:n.*1481_*1482insACAGG
XM_006718075.4:c.*1481_*1482insACAGG XP_006718138.1:n.*1481_*1482insACAGG
XM_011540369.2:c.*1481_*1482insACAGG XP_011538671.1:n.*1481_*1482insACAGG
NM_004273.5:c.*1481_*1482insACAGG MANE Select NP_004264.2:n.*1481_*1482insACAGG