Canonical Allele Identifier: CA668113048
Gene: CHST3 HGNC NCBI

Linked Data

dbSNP Id: rs1045788383
gnomAD v3: 10-72009649-GC-G
gnomAD v4: 10-72009649-GC-G
MyVariant Identifiers: chr10:g.73769408del (hg19) chr10:g.72009650del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.72009656del , CM000672.2:g.72009656del GRCh38
NC_000010.10:g.73769414del , CM000672.1:g.73769414del GRCh37
NC_000010.9:g.73439420del NCBI36
NG_012635.1:g.50295del

Transcript Alleles

HGVS Amino-acid Change
ENST00000373115.5:c.*1185del MANE Select ENSP00000362207.4:n.*1185del
ENST00000373115.4:c.*1185del ENSP00000362207.4:n.*1185del
NM_004273.4:c.*1185del NP_004264.2:n.*1185del
XM_006718075.2:c.*1185del XP_006718138.1:n.*1185del
XM_011540369.1:c.*1185del XP_011538671.1:n.*1185del
XM_006718075.4:c.*1185del XP_006718138.1:n.*1185del
XM_011540369.2:c.*1185del XP_011538671.1:n.*1185del
NM_004273.5:c.*1185del MANE Select NP_004264.2:n.*1185del
Search 100 bp 5'
Search 100 bp 3'