Canonical Allele Identifier: CA2609582372

Gene: CHST3

Linked Data

• gnomAD v4: 10-72007947-GTGCT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.72007948_72007951del , CM000672.2:g.72007948_72007951del	GRCh38
NC_000010.10:g.73767706_73767709del , CM000672.1:g.73767706_73767709del	GRCh37
NC_000010.9:g.73437712_73437715del	NCBI36
NG_012635.1:g.48587_48590del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373115.5:c.917_920del MANE Select	ENSP00000362207.4:p.Val306GlyfsTer27
ENST00000373115.4:c.917_920del	ENSP00000362207.4:p.Val306GlyfsTer27
NM_004273.4:c.917_920del	NP_004264.2:p.Val306GlyfsTer27
XM_006718075.2:c.917_920del	XP_006718138.1:p.Val306GlyfsTer27
XM_011540369.1:c.917_920del	XP_011538671.1:p.Val306GlyfsTer27
XM_006718075.4:c.917_920del	XP_006718138.1:p.Val306GlyfsTer27
XM_011540369.2:c.917_920del	XP_011538671.1:p.Val306GlyfsTer27
NM_004273.5:c.917_920del MANE Select	NP_004264.2:p.Val306GlyfsTer27