Canonical Allele Identifier: CA2788492388

Gene: CHST3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.72008258_72008259insAG , CM000672.2:g.72008258_72008259insAG	GRCh38
NC_000010.10:g.73768016_73768017insAG , CM000672.1:g.73768016_73768017insAG	GRCh37
NC_000010.9:g.73438022_73438023insAG	NCBI36
NG_012635.1:g.48897_48898insAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373115.5:c.1227_1228insAG MANE Select	ENSP00000362207.4:p.Asp410ArgfsTer?
ENST00000373115.4:c.1227_1228insAG	ENSP00000362207.4:p.Asp410ArgfsTer?
NM_004273.4:c.1227_1228insAG	NP_004264.2:p.Asp410ArgfsTer?
XM_006718075.2:c.1227_1228insAG	XP_006718138.1:p.Asp410ArgfsTer?
XM_011540369.1:c.1227_1228insAG	XP_011538671.1:p.Asp410ArgfsTer?
XM_006718075.4:c.1227_1228insAG	XP_006718138.1:p.Asp410ArgfsTer?
XM_011540369.2:c.1227_1228insAG	XP_011538671.1:p.Asp410ArgfsTer?
NM_004273.5:c.1227_1228insAG MANE Select	NP_004264.2:p.Asp410ArgfsTer?