Canonical Allele Identifier: CA3036863830
Community Standard Title: NM_004273.5(CHST3):c.*4258_*4331del
Gene: CHST3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.72012729_72012802del , CM000672.2:g.72012729_72012802del GRCh38
NC_000010.10:g.73772487_73772560del , CM000672.1:g.73772487_73772560del GRCh37
NC_000010.9:g.73442493_73442566del NCBI36
NG_012635.1:g.53368_53441del

Transcript Alleles

HGVS Amino-acid Change
NM_004273.5:c.*4258_*4331del MANE Select NP_004264.2:n.*4258_*4331del
ENST00000373115.5:c.*4258_*4331del MANE Select ENSP00000362207.4:n.*4258_*4331del
NM_004273.4:c.*4258_*4331del NP_004264.2:n.*4258_*4331del
ENST00000373115.4:c.*4258_*4331del ENSP00000362207.4:n.*4258_*4331del
XM_006718075.2:c.*4258_*4331del XP_006718138.1:n.*4258_*4331del
XM_006718075.4:c.*4258_*4331del XP_006718138.1:n.*4258_*4331del
XM_011540369.1:c.*4258_*4331del XP_011538671.1:n.*4258_*4331del
XM_011540369.2:c.*4258_*4331del XP_011538671.1:n.*4258_*4331del