Canonical Allele Identifier: CA2722101866

Gene: CHST3

Linked Data

• dbSNP Id: rs2131775034

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.72007594_72007596del , CM000672.2:g.72007594_72007596del	GRCh38
NC_000010.10:g.73767352_73767354del , CM000672.1:g.73767352_73767354del	GRCh37
NC_000010.9:g.73437358_73437360del	NCBI36
NG_012635.1:g.48233_48235del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373115.5:c.563_565del MANE Select	ENSP00000362207.4:p.Tyr188_Arg189delinsCys
ENST00000373115.4:c.563_565del	ENSP00000362207.4:p.Tyr188_Arg189delinsCys
NM_004273.4:c.563_565del	NP_004264.2:p.Tyr188_Arg189delinsCys
XM_006718075.2:c.563_565del	XP_006718138.1:p.Tyr188_Arg189delinsCys
XM_011540369.1:c.563_565del	XP_011538671.1:p.Tyr188_Arg189delinsCys
XM_006718075.4:c.563_565del	XP_006718138.1:p.Tyr188_Arg189delinsCys
XM_011540369.2:c.563_565del	XP_011538671.1:p.Tyr188_Arg189delinsCys
NM_004273.5:c.563_565del MANE Select	NP_004264.2:p.Tyr188_Arg189delinsCys