Canonical Allele Identifier: CA2722111430
Gene: CHST3 HGNC NCBI

Linked Data

dbSNP Id: rs2131779033

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.72009766_72009767dup , CM000672.2:g.72009766_72009767dup GRCh38
NC_000010.10:g.73769524_73769525dup , CM000672.1:g.73769524_73769525dup GRCh37
NC_000010.9:g.73439530_73439531dup NCBI36
NG_012635.1:g.50405_50406dup

Transcript Alleles

HGVS Amino-acid change
ENST00000373115.5:c.*1295_*1296dup MANE Select ENSP00000362207.4:n.*1295_*1296dup
ENST00000373115.4:c.*1295_*1296dup ENSP00000362207.4:n.*1295_*1296dup
NM_004273.4:c.*1295_*1296dup NP_004264.2:n.*1295_*1296dup
XM_006718075.2:c.*1295_*1296dup XP_006718138.1:n.*1295_*1296dup
XM_011540369.1:c.*1295_*1296dup XP_011538671.1:n.*1295_*1296dup
XM_006718075.4:c.*1295_*1296dup XP_006718138.1:n.*1295_*1296dup
XM_011540369.2:c.*1295_*1296dup XP_011538671.1:n.*1295_*1296dup
NM_004273.5:c.*1295_*1296dup MANE Select NP_004264.2:n.*1295_*1296dup