Canonical Allele Identifier: CA2609586648
Gene: CHST3 HGNC NCBI

Linked Data

gnomAD v4: 10-72009246-AGG-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.72009247_72009248del , CM000672.2:g.72009247_72009248del GRCh38
NC_000010.10:g.73769005_73769006del , CM000672.1:g.73769005_73769006del GRCh37
NC_000010.9:g.73439011_73439012del NCBI36
NG_012635.1:g.49886_49887del

Transcript Alleles

HGVS Amino-acid Change
ENST00000373115.5:c.*776_*777del MANE Select ENSP00000362207.4:n.*776_*777del
ENST00000373115.4:c.*776_*777del ENSP00000362207.4:n.*776_*777del
NM_004273.4:c.*776_*777del NP_004264.2:n.*776_*777del
XM_006718075.2:c.*776_*777del XP_006718138.1:n.*776_*777del
XM_011540369.1:c.*776_*777del XP_011538671.1:n.*776_*777del
XM_006718075.4:c.*776_*777del XP_006718138.1:n.*776_*777del
XM_011540369.2:c.*776_*777del XP_011538671.1:n.*776_*777del
NM_004273.5:c.*776_*777del MANE Select NP_004264.2:n.*776_*777del
Search 100 bp 5'
Search 100 bp 3'