Canonical Allele Identifier: CA2788492444

Gene: CHST3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.72010004_72010013del , CM000672.2:g.72010004_72010013del	GRCh38
NC_000010.10:g.73769762_73769771del , CM000672.1:g.73769762_73769771del	GRCh37
NC_000010.9:g.73439768_73439777del	NCBI36
NG_012635.1:g.50643_50652del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373115.5:c.*1533_*1542del MANE Select	ENSP00000362207.4:n.*1533_*1542del
ENST00000373115.4:c.*1533_*1542del	ENSP00000362207.4:n.*1533_*1542del
NM_004273.4:c.*1533_*1542del	NP_004264.2:n.*1533_*1542del
XM_006718075.2:c.*1533_*1542del	XP_006718138.1:n.*1533_*1542del
XM_011540369.1:c.*1533_*1542del	XP_011538671.1:n.*1533_*1542del
XM_006718075.4:c.*1533_*1542del	XP_006718138.1:n.*1533_*1542del
XM_011540369.2:c.*1533_*1542del	XP_011538671.1:n.*1533_*1542del
NM_004273.5:c.*1533_*1542del MANE Select	NP_004264.2:n.*1533_*1542del