Canonical Allele Identifier: CA2609588196
Gene: CHST3 HGNC NCBI

Linked Data

gnomAD v4: 10-72009977-GA-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.72009978del , CM000672.2:g.72009978del GRCh38
NC_000010.10:g.73769736del , CM000672.1:g.73769736del GRCh37
NC_000010.9:g.73439742del NCBI36
NG_012635.1:g.50617del

Transcript Alleles

HGVS Amino-acid Change
ENST00000373115.5:c.*1507del MANE Select ENSP00000362207.4:n.*1507del
ENST00000373115.4:c.*1507del ENSP00000362207.4:n.*1507del
NM_004273.4:c.*1507del NP_004264.2:n.*1507del
XM_006718075.2:c.*1507del XP_006718138.1:n.*1507del
XM_011540369.1:c.*1507del XP_011538671.1:n.*1507del
XM_006718075.4:c.*1507del XP_006718138.1:n.*1507del
XM_011540369.2:c.*1507del XP_011538671.1:n.*1507del
NM_004273.5:c.*1507del MANE Select NP_004264.2:n.*1507del
Search 100 bp 5'
Search 100 bp 3'