Canonical Allele Identifier: CA2609587555

Gene: CHST3

Linked Data

• gnomAD v4: 10-72009709-G-GA

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.72009709_72009710insA , CM000672.2:g.72009709_72009710insA	GRCh38
NC_000010.10:g.73769467_73769468insA , CM000672.1:g.73769467_73769468insA	GRCh37
NC_000010.9:g.73439473_73439474insA	NCBI36
NG_012635.1:g.50348_50349insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373115.5:c.*1238_*1239insA MANE Select	ENSP00000362207.4:n.*1238_*1239insA
ENST00000373115.4:c.*1238_*1239insA	ENSP00000362207.4:n.*1238_*1239insA
NM_004273.4:c.*1238_*1239insA	NP_004264.2:n.*1238_*1239insA
XM_006718075.2:c.*1238_*1239insA	XP_006718138.1:n.*1238_*1239insA
XM_011540369.1:c.*1238_*1239insA	XP_011538671.1:n.*1238_*1239insA
XM_006718075.4:c.*1238_*1239insA	XP_006718138.1:n.*1238_*1239insA
XM_011540369.2:c.*1238_*1239insA	XP_011538671.1:n.*1238_*1239insA
NM_004273.5:c.*1238_*1239insA MANE Select	NP_004264.2:n.*1238_*1239insA