Canonical Allele Identifier: CA377145070

Gene: CHST3

Linked Data

• MyVariant Identifiers: chr10:g.73767385A>T (hg19) ; chr10:g.72007627A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.72007627A>T , CM000672.2:g.72007627A>T	GRCh38
NC_000010.10:g.73767385A>T , CM000672.1:g.73767385A>T	GRCh37
NC_000010.9:g.73437391A>T	NCBI36
NG_012635.1:g.48266A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373115.5:c.596A>T MANE Select	ENSP00000362207.4:p.Asp199Val
ENST00000373115.4:c.596A>T	ENSP00000362207.4:p.Asp199Val
NM_004273.4:c.596A>T	NP_004264.2:p.Asp199Val
XM_006718075.2:c.596A>T	XP_006718138.1:p.Asp199Val
XM_011540369.1:c.596A>T	XP_011538671.1:p.Asp199Val
XM_006718075.4:c.596A>T	XP_006718138.1:p.Asp199Val
XM_011540369.2:c.596A>T	XP_011538671.1:p.Asp199Val
NM_004273.5:c.596A>T MANE Select	NP_004264.2:p.Asp199Val