Canonical Allele Identifier: CA1918977354
Gene: CHST3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.72009266_72009267delinsGC , CM000672.2:g.72009266_72009267delinsGC GRCh38
NC_000010.10:g.73769024_73769025delinsGC , CM000672.1:g.73769024_73769025delinsGC GRCh37
NC_000010.9:g.73439030_73439031delinsGC NCBI36
NG_012635.1:g.49905_49906delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000373115.5:c.*795_*796delinsGC MANE Select ENSP00000362207.4:n.*795_*796delinsGC
ENST00000373115.4:c.*795_*796delinsGC ENSP00000362207.4:n.*795_*796delinsGC
NM_004273.4:c.*795_*796delinsGC NP_004264.2:n.*795_*796delinsGC
XM_006718075.2:c.*795_*796delinsGC XP_006718138.1:n.*795_*796delinsGC
XM_011540369.1:c.*795_*796delinsGC XP_011538671.1:n.*795_*796delinsGC
XM_006718075.4:c.*795_*796delinsGC XP_006718138.1:n.*795_*796delinsGC
XM_011540369.2:c.*795_*796delinsGC XP_011538671.1:n.*795_*796delinsGC
NM_004273.5:c.*795_*796delinsGC MANE Select NP_004264.2:n.*795_*796delinsGC