Canonical Allele Identifier: CA2788492441

Gene: CHST3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.72009991_72009992insTA , CM000672.2:g.72009991_72009992insTA	GRCh38
NC_000010.10:g.73769749_73769750insTA , CM000672.1:g.73769749_73769750insTA	GRCh37
NC_000010.9:g.73439755_73439756insTA	NCBI36
NG_012635.1:g.50630_50631insTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373115.5:c.*1520_*1521insTA MANE Select	ENSP00000362207.4:n.*1520_*1521insTA
ENST00000373115.4:c.*1520_*1521insTA	ENSP00000362207.4:n.*1520_*1521insTA
NM_004273.4:c.*1520_*1521insTA	NP_004264.2:n.*1520_*1521insTA
XM_006718075.2:c.*1520_*1521insTA	XP_006718138.1:n.*1520_*1521insTA
XM_011540369.1:c.*1520_*1521insTA	XP_011538671.1:n.*1520_*1521insTA
XM_006718075.4:c.*1520_*1521insTA	XP_006718138.1:n.*1520_*1521insTA
XM_011540369.2:c.*1520_*1521insTA	XP_011538671.1:n.*1520_*1521insTA
NM_004273.5:c.*1520_*1521insTA MANE Select	NP_004264.2:n.*1520_*1521insTA