Canonical Allele Identifier: CA2788492386
Gene: CHST3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.72008252_72008253del , CM000672.2:g.72008252_72008253del GRCh38
NC_000010.10:g.73768010_73768011del , CM000672.1:g.73768010_73768011del GRCh37
NC_000010.9:g.73438016_73438017del NCBI36
NG_012635.1:g.48891_48892del

Transcript Alleles

HGVS Amino-acid Change
ENST00000373115.5:c.1221_1222del MANE Select ENSP00000362207.4:p.Ala408ProfsTer?
ENST00000373115.4:c.1221_1222del ENSP00000362207.4:p.Ala408ProfsTer?
NM_004273.4:c.1221_1222del NP_004264.2:p.Ala408ProfsTer?
XM_006718075.2:c.1221_1222del XP_006718138.1:p.Ala408ProfsTer?
XM_011540369.1:c.1221_1222del XP_011538671.1:p.Ala408ProfsTer?
XM_006718075.4:c.1221_1222del XP_006718138.1:p.Ala408ProfsTer?
XM_011540369.2:c.1221_1222del XP_011538671.1:p.Ala408ProfsTer?
NM_004273.5:c.1221_1222del MANE Select NP_004264.2:p.Ala408ProfsTer?