Canonical Allele Identifier: CA2609581014

Gene: CHST3

Linked Data

• gnomAD v4: 10-72007578-G-GGCTCGGCCCTGGTGTACCGCGACGT

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.72007583_72007607dup , CM000672.2:g.72007583_72007607dup	GRCh38
NC_000010.10:g.73767341_73767365dup , CM000672.1:g.73767341_73767365dup	GRCh37
NC_000010.9:g.73437347_73437371dup	NCBI36
NG_012635.1:g.48222_48246dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373115.5:c.552_576dup MANE Select	ENSP00000362207.4:p.Lys193GlyfsTer?
ENST00000373115.4:c.552_576dup	ENSP00000362207.4:p.Lys193GlyfsTer?
NM_004273.4:c.552_576dup	NP_004264.2:p.Lys193GlyfsTer?
XM_006718075.2:c.552_576dup	XP_006718138.1:p.Lys193GlyfsTer?
XM_011540369.1:c.552_576dup	XP_011538671.1:p.Lys193GlyfsTer?
XM_006718075.4:c.552_576dup	XP_006718138.1:p.Lys193GlyfsTer?
XM_011540369.2:c.552_576dup	XP_011538671.1:p.Lys193GlyfsTer?
NM_004273.5:c.552_576dup MANE Select	NP_004264.2:p.Lys193GlyfsTer?