Canonical Allele Identifier: CA2609582012
Gene: CHST3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.72007809del , CM000672.2:g.72007809del GRCh38
NC_000010.10:g.73767567del , CM000672.1:g.73767567del GRCh37
NC_000010.9:g.73437573del NCBI36
NG_012635.1:g.48448del

Transcript Alleles

HGVS Amino-acid change
ENST00000373115.5:c.778del MANE Select ENSP00000362207.4:p.Ala260ProfsTer?
ENST00000373115.4:c.778del ENSP00000362207.4:p.Ala260ProfsTer?
NM_004273.4:c.778del NP_004264.2:p.Ala260ProfsTer?
XM_006718075.2:c.778del XP_006718138.1:p.Ala260ProfsTer?
XM_011540369.1:c.778del XP_011538671.1:p.Ala260ProfsTer?
XM_006718075.4:c.778del XP_006718138.1:p.Ala260ProfsTer?
XM_011540369.2:c.778del XP_011538671.1:p.Ala260ProfsTer?
NM_004273.5:c.778del MANE Select NP_004264.2:p.Ala260ProfsTer?