Canonical Allele Identifier: CA2788492443
Gene: CHST3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.72009996_72009999del , CM000672.2:g.72009996_72009999del GRCh38
NC_000010.10:g.73769754_73769757del , CM000672.1:g.73769754_73769757del GRCh37
NC_000010.9:g.73439760_73439763del NCBI36
NG_012635.1:g.50635_50638del

Transcript Alleles

HGVS Amino-acid Change
ENST00000373115.5:c.*1525_*1528del MANE Select ENSP00000362207.4:n.*1525_*1528del
ENST00000373115.4:c.*1525_*1528del ENSP00000362207.4:n.*1525_*1528del
NM_004273.4:c.*1525_*1528del NP_004264.2:n.*1525_*1528del
XM_006718075.2:c.*1525_*1528del XP_006718138.1:n.*1525_*1528del
XM_011540369.1:c.*1525_*1528del XP_011538671.1:n.*1525_*1528del
XM_006718075.4:c.*1525_*1528del XP_006718138.1:n.*1525_*1528del
XM_011540369.2:c.*1525_*1528del XP_011538671.1:n.*1525_*1528del
NM_004273.5:c.*1525_*1528del MANE Select NP_004264.2:n.*1525_*1528del