Canonical Allele Identifier: CA1918977656

Gene: CHST3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.72009840_72009841delinsTG , CM000672.2:g.72009840_72009841delinsTG	GRCh38
NC_000010.10:g.73769598_73769599delinsTG , CM000672.1:g.73769598_73769599delinsTG	GRCh37
NC_000010.9:g.73439604_73439605delinsTG	NCBI36
NG_012635.1:g.50479_50480delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373115.5:c.*1369_*1370delinsTG MANE Select	ENSP00000362207.4:n.*1369_*1370delinsTG
ENST00000373115.4:c.*1369_*1370delinsTG	ENSP00000362207.4:n.*1369_*1370delinsTG
NM_004273.4:c.*1369_*1370delinsTG	NP_004264.2:n.*1369_*1370delinsTG
XM_006718075.2:c.*1369_*1370delinsTG	XP_006718138.1:n.*1369_*1370delinsTG
XM_011540369.1:c.*1369_*1370delinsTG	XP_011538671.1:n.*1369_*1370delinsTG
XM_006718075.4:c.*1369_*1370delinsTG	XP_006718138.1:n.*1369_*1370delinsTG
XM_011540369.2:c.*1369_*1370delinsTG	XP_011538671.1:n.*1369_*1370delinsTG
NM_004273.5:c.*1369_*1370delinsTG MANE Select	NP_004264.2:n.*1369_*1370delinsTG