Canonical Allele Identifier: CA2609583303
Gene: CHST3 HGNC NCBI

Linked Data

gnomAD v4: 10-72008155-CACGCGGG-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.72008156_72008162del , CM000672.2:g.72008156_72008162del GRCh38
NC_000010.10:g.73767914_73767920del , CM000672.1:g.73767914_73767920del GRCh37
NC_000010.9:g.73437920_73437926del NCBI36
NG_012635.1:g.48795_48801del

Transcript Alleles

HGVS Amino-acid Change
ENST00000373115.5:c.1125_1131del MANE Select ENSP00000362207.4:p.Gly377CysfsTer15
ENST00000373115.4:c.1125_1131del ENSP00000362207.4:p.Gly377CysfsTer15
NM_004273.4:c.1125_1131del NP_004264.2:p.Gly377CysfsTer15
XM_006718075.2:c.1125_1131del XP_006718138.1:p.Gly377CysfsTer15
XM_011540369.1:c.1125_1131del XP_011538671.1:p.Gly377CysfsTer15
XM_006718075.4:c.1125_1131del XP_006718138.1:p.Gly377CysfsTer15
XM_011540369.2:c.1125_1131del XP_011538671.1:p.Gly377CysfsTer15
NM_004273.5:c.1125_1131del MANE Select NP_004264.2:p.Gly377CysfsTer15
Search 100 bp 5'
Search 100 bp 3'