Canonical Allele Identifier: CA2609582327
Gene: CHST3 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000373115.5:c.910del MANE Select ENSP00000362207.4:p.Arg304GlyfsTer30
ENST00000373115.4:c.910del ENSP00000362207.4:p.Arg304GlyfsTer30
NM_004273.4:c.910del NP_004264.2:p.Arg304GlyfsTer30
XM_006718075.2:c.910del XP_006718138.1:p.Arg304GlyfsTer30
XM_011540369.1:c.910del XP_011538671.1:p.Arg304GlyfsTer30
XM_006718075.4:c.910del XP_006718138.1:p.Arg304GlyfsTer30
XM_011540369.2:c.910del XP_011538671.1:p.Arg304GlyfsTer30
NM_004273.5:c.910del MANE Select NP_004264.2:p.Arg304GlyfsTer30