Canonical Allele Identifier: CA1918977429
Gene: CHST3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.72009405_72009407delinsCCA , CM000672.2:g.72009405_72009407delinsCCA GRCh38
NC_000010.10:g.73769163_73769165delinsCCA , CM000672.1:g.73769163_73769165delinsCCA GRCh37
NC_000010.9:g.73439169_73439171delinsCCA NCBI36
NG_012635.1:g.50044_50046delinsCCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000373115.5:c.*934_*936delinsCCA MANE Select ENSP00000362207.4:n.*934_*936delinsCCA
ENST00000373115.4:c.*934_*936delinsCCA ENSP00000362207.4:n.*934_*936delinsCCA
NM_004273.4:c.*934_*936delinsCCA NP_004264.2:n.*934_*936delinsCCA
XM_006718075.2:c.*934_*936delinsCCA XP_006718138.1:n.*934_*936delinsCCA
XM_011540369.1:c.*934_*936delinsCCA XP_011538671.1:n.*934_*936delinsCCA
XM_006718075.4:c.*934_*936delinsCCA XP_006718138.1:n.*934_*936delinsCCA
XM_011540369.2:c.*934_*936delinsCCA XP_011538671.1:n.*934_*936delinsCCA
NM_004273.5:c.*934_*936delinsCCA MANE Select NP_004264.2:n.*934_*936delinsCCA