Canonical Allele Identifier: CA2788492303

Gene: CHST3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.72007647_72007655del , CM000672.2:g.72007647_72007655del	GRCh38
NC_000010.10:g.73767405_73767413del , CM000672.1:g.73767405_73767413del	GRCh37
NC_000010.9:g.73437411_73437419del	NCBI36
NG_012635.1:g.48286_48294del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373115.5:c.616_624del MANE Select	ENSP00000362207.4:p.Phe206_Thr208del
ENST00000373115.4:c.616_624del	ENSP00000362207.4:p.Phe206_Thr208del
NM_004273.4:c.616_624del	NP_004264.2:p.Phe206_Thr208del
XM_006718075.2:c.616_624del	XP_006718138.1:p.Phe206_Thr208del
XM_011540369.1:c.616_624del	XP_011538671.1:p.Phe206_Thr208del
XM_006718075.4:c.616_624del	XP_006718138.1:p.Phe206_Thr208del
XM_011540369.2:c.616_624del	XP_011538671.1:p.Phe206_Thr208del
NM_004273.5:c.616_624del MANE Select	NP_004264.2:p.Phe206_Thr208del