Canonical Allele Identifier: CA2609582395

Gene: CHST3

Linked Data

• gnomAD v4: 10-72007954-CCTCGCGCATGG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.72007955_72007965del , CM000672.2:g.72007955_72007965del	GRCh38
NC_000010.10:g.73767713_73767723del , CM000672.1:g.73767713_73767723del	GRCh37
NC_000010.9:g.73437719_73437729del	NCBI36
NG_012635.1:g.48594_48604del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373115.5:c.924_934del MANE Select	ENSP00000362207.4:p.Ser309GlyfsTer7
ENST00000373115.4:c.924_934del	ENSP00000362207.4:p.Ser309GlyfsTer7
NM_004273.4:c.924_934del	NP_004264.2:p.Ser309GlyfsTer7
XM_006718075.2:c.924_934del	XP_006718138.1:p.Ser309GlyfsTer7
XM_011540369.1:c.924_934del	XP_011538671.1:p.Ser309GlyfsTer7
XM_006718075.4:c.924_934del	XP_006718138.1:p.Ser309GlyfsTer7
XM_011540369.2:c.924_934del	XP_011538671.1:p.Ser309GlyfsTer7
NM_004273.5:c.924_934del MANE Select	NP_004264.2:p.Ser309GlyfsTer7