Canonical Allele Identifier: CA2609583938
Gene: CHST3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.72008261del , CM000672.2:g.72008261del GRCh38
NC_000010.10:g.73768019del , CM000672.1:g.73768019del GRCh37
NC_000010.9:g.73438025del NCBI36
NG_012635.1:g.48900del

Transcript Alleles

HGVS Amino-acid Change
ENST00000373115.5:c.1230del MANE Select ENSP00000362207.4:p.Asp410GlufsTer?
ENST00000373115.4:c.1230del ENSP00000362207.4:p.Asp410GlufsTer?
NM_004273.4:c.1230del NP_004264.2:p.Asp410GlufsTer?
XM_006718075.2:c.1230del XP_006718138.1:p.Asp410GlufsTer?
XM_011540369.1:c.1230del XP_011538671.1:p.Asp410GlufsTer?
XM_006718075.4:c.1230del XP_006718138.1:p.Asp410GlufsTer?
XM_011540369.2:c.1230del XP_011538671.1:p.Asp410GlufsTer?
NM_004273.5:c.1230del MANE Select NP_004264.2:p.Asp410GlufsTer?