Canonical Allele Identifier: CA2609582334
Gene: CHST3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.72007941dup , CM000672.2:g.72007941dup GRCh38
NC_000010.10:g.73767699dup , CM000672.1:g.73767699dup GRCh37
NC_000010.9:g.73437705dup NCBI36
NG_012635.1:g.48580dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000373115.5:c.910dup MANE Select ENSP00000362207.4:p.Arg304ProfsTer16
ENST00000373115.4:c.910dup ENSP00000362207.4:p.Arg304ProfsTer16
NM_004273.4:c.910dup NP_004264.2:p.Arg304ProfsTer16
XM_006718075.2:c.910dup XP_006718138.1:p.Arg304ProfsTer16
XM_011540369.1:c.910dup XP_011538671.1:p.Arg304ProfsTer16
XM_006718075.4:c.910dup XP_006718138.1:p.Arg304ProfsTer16
XM_011540369.2:c.910dup XP_011538671.1:p.Arg304ProfsTer16
NM_004273.5:c.910dup MANE Select NP_004264.2:p.Arg304ProfsTer16