Canonical Allele Identifier: CA668112780

Gene: CHST3

Linked Data

• dbSNP Id: rs1372740023
• gnomAD v3: 10-72009301-GAC-G
• gnomAD v4: 10-72009301-GAC-G
• MyVariant Identifiers: chr10:g.73769060_73769061del (hg19) ; chr10:g.72009302_72009303del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.72009305_72009306del , CM000672.2:g.72009305_72009306del	GRCh38
NC_000010.10:g.73769063_73769064del , CM000672.1:g.73769063_73769064del	GRCh37
NC_000010.9:g.73439069_73439070del	NCBI36
NG_012635.1:g.49944_49945del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373115.5:c.*834_*835del MANE Select	ENSP00000362207.4:n.*834_*835del
ENST00000373115.4:c.*834_*835del	ENSP00000362207.4:n.*834_*835del
NM_004273.4:c.*834_*835del	NP_004264.2:n.*834_*835del
XM_006718075.2:c.*834_*835del	XP_006718138.1:n.*834_*835del
XM_011540369.1:c.*834_*835del	XP_011538671.1:n.*834_*835del
XM_006718075.4:c.*834_*835del	XP_006718138.1:n.*834_*835del
XM_011540369.2:c.*834_*835del	XP_011538671.1:n.*834_*835del
NM_004273.5:c.*834_*835del MANE Select	NP_004264.2:n.*834_*835del