Canonical Allele Identifier: CA1918976799

Gene: CHST3

Linked Data

• dbSNP Id: rs1840067346

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.72008209del , CM000672.2:g.72008209del	GRCh38
NC_000010.10:g.73767967del , CM000672.1:g.73767967del	GRCh37
NC_000010.9:g.73437973del	NCBI36
NG_012635.1:g.48848del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373115.5:c.1178del MANE Select	ENSP00000362207.4:p.Leu393ArgfsTer?
ENST00000373115.4:c.1178del	ENSP00000362207.4:p.Leu393ArgfsTer?
NM_004273.4:c.1178del	NP_004264.2:p.Leu393ArgfsTer?
XM_006718075.2:c.1178del	XP_006718138.1:p.Leu393ArgfsTer?
XM_011540369.1:c.1178del	XP_011538671.1:p.Leu393ArgfsTer?
XM_006718075.4:c.1178del	XP_006718138.1:p.Leu393ArgfsTer?
XM_011540369.2:c.1178del	XP_011538671.1:p.Leu393ArgfsTer?
NM_004273.5:c.1178del MANE Select	NP_004264.2:p.Leu393ArgfsTer?