Canonical Allele Identifier: CA1918977545
Gene: CHST3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.72009633_72009634delinsGA , CM000672.2:g.72009633_72009634delinsGA GRCh38
NC_000010.10:g.73769391_73769392delinsGA , CM000672.1:g.73769391_73769392delinsGA GRCh37
NC_000010.9:g.73439397_73439398delinsGA NCBI36
NG_012635.1:g.50272_50273delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000373115.5:c.*1162_*1163delinsGA MANE Select ENSP00000362207.4:n.*1162_*1163delinsGA
ENST00000373115.4:c.*1162_*1163delinsGA ENSP00000362207.4:n.*1162_*1163delinsGA
NM_004273.4:c.*1162_*1163delinsGA NP_004264.2:n.*1162_*1163delinsGA
XM_006718075.2:c.*1162_*1163delinsGA XP_006718138.1:n.*1162_*1163delinsGA
XM_011540369.1:c.*1162_*1163delinsGA XP_011538671.1:n.*1162_*1163delinsGA
XM_006718075.4:c.*1162_*1163delinsGA XP_006718138.1:n.*1162_*1163delinsGA
XM_011540369.2:c.*1162_*1163delinsGA XP_011538671.1:n.*1162_*1163delinsGA
NM_004273.5:c.*1162_*1163delinsGA MANE Select NP_004264.2:n.*1162_*1163delinsGA