Canonical Allele Identifier: CA1918976399

Gene: CHST3

Linked Data

• dbSNP Id: rs1840060355

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.72007845dup , CM000672.2:g.72007845dup	GRCh38
NC_000010.10:g.73767603dup , CM000672.1:g.73767603dup	GRCh37
NC_000010.9:g.73437609dup	NCBI36
NG_012635.1:g.48484dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373115.5:c.814dup MANE Select	ENSP00000362207.4:p.Leu272ProfsTer?
ENST00000373115.4:c.814dup	ENSP00000362207.4:p.Leu272ProfsTer?
NM_004273.4:c.814dup	NP_004264.2:p.Leu272ProfsTer?
XM_006718075.2:c.814dup	XP_006718138.1:p.Leu272ProfsTer?
XM_011540369.1:c.814dup	XP_011538671.1:p.Leu272ProfsTer?
XM_006718075.4:c.814dup	XP_006718138.1:p.Leu272ProfsTer?
XM_011540369.2:c.814dup	XP_011538671.1:p.Leu272ProfsTer?
NM_004273.5:c.814dup MANE Select	NP_004264.2:p.Leu272ProfsTer?