Canonical Allele Identifier: CA929816585
Gene: CHST3 HGNC NCBI

Linked Data

dbSNP Id: rs1840082755
gnomAD v3: 10-72009258-AG-A
gnomAD v4: 10-72009258-AG-A
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.72009261del , CM000672.2:g.72009261del GRCh38
NC_000010.10:g.73769019del , CM000672.1:g.73769019del GRCh37
NC_000010.9:g.73439025del NCBI36
NG_012635.1:g.49900del

Transcript Alleles

HGVS Amino-acid Change
ENST00000373115.5:c.*790del MANE Select ENSP00000362207.4:n.*790del
ENST00000373115.4:c.*790del ENSP00000362207.4:n.*790del
NM_004273.4:c.*790del NP_004264.2:n.*790del
XM_006718075.2:c.*790del XP_006718138.1:n.*790del
XM_011540369.1:c.*790del XP_011538671.1:n.*790del
XM_006718075.4:c.*790del XP_006718138.1:n.*790del
XM_011540369.2:c.*790del XP_011538671.1:n.*790del
NM_004273.5:c.*790del MANE Select NP_004264.2:n.*790del
Search 100 bp 5'
Search 100 bp 3'