Canonical Allele Identifier: CA2574581834
Gene: CHST3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.72007918_72007935del , CM000672.2:g.72007918_72007935del GRCh38
NC_000010.10:g.73767676_73767693del , CM000672.1:g.73767676_73767693del GRCh37
NC_000010.9:g.73437682_73437699del NCBI36
NG_012635.1:g.48557_48574del

Transcript Alleles

HGVS Amino-acid Change
ENST00000373115.5:c.887_904del MANE Select ENSP00000362207.4:p.Val296_Arg301del
ENST00000373115.4:c.887_904del ENSP00000362207.4:p.Val296_Arg301del
NM_004273.4:c.887_904del NP_004264.2:p.Val296_Arg301del
XM_006718075.2:c.887_904del XP_006718138.1:p.Val296_Arg301del
XM_011540369.1:c.887_904del XP_011538671.1:p.Val296_Arg301del
XM_006718075.4:c.887_904del XP_006718138.1:p.Val296_Arg301del
XM_011540369.2:c.887_904del XP_011538671.1:p.Val296_Arg301del
NM_004273.5:c.887_904del MANE Select NP_004264.2:p.Val296_Arg301del