Canonical Allele Identifier: CA1918977618
Gene: CHST3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.72009773_72009782delinsAGGATGTGCT , CM000672.2:g.72009773_72009782delinsAGGATGTGCT GRCh38
NC_000010.10:g.73769531_73769540delinsAGGATGTGCT , CM000672.1:g.73769531_73769540delinsAGGATGTGCT GRCh37
NC_000010.9:g.73439537_73439546delinsAGGATGTGCT NCBI36
NG_012635.1:g.50412_50421delinsAGGATGTGCT

Transcript Alleles

HGVS Amino-acid change
ENST00000373115.5:c.*1302_*1311delinsAGGATGTGCT MANE Select ENSP00000362207.4:n.*1302_*1311delinsAGGA...
ENST00000373115.4:c.*1302_*1311delinsAGGATGTGCT ENSP00000362207.4:n.*1302_*1311delinsAGGA...
NM_004273.4:c.*1302_*1311delinsAGGATGTGCT NP_004264.2:n.*1302_*1311delinsAGGATGTGCT...
XM_006718075.2:c.*1302_*1311delinsAGGATGTGCT XP_006718138.1:n.*1302_*1311delinsAGGATGT...
XM_011540369.1:c.*1302_*1311delinsAGGATGTGCT XP_011538671.1:n.*1302_*1311delinsAGGATGT...
XM_006718075.4:c.*1302_*1311delinsAGGATGTGCT XP_006718138.1:n.*1302_*1311delinsAGGATGT...
XM_011540369.2:c.*1302_*1311delinsAGGATGTGCT XP_011538671.1:n.*1302_*1311delinsAGGATGT...
NM_004273.5:c.*1302_*1311delinsAGGATGTGCT MANE Select NP_004264.2:n.*1302_*1311delinsAGGATGTGCT...