Canonical Allele Identifier: CA136915009

Gene: DXO

Linked Data

• dbSNP Id: rs372370078
• gnomAD v4: 6-31969862-C-T
• MyVariant Identifiers: chr6:g.31969862C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31969862C>T , CM000668.2:g.31969862C>T	GRCh38
NC_000006.11:g.31937639C>T , CM000668.1:g.31937639C>T	GRCh37
NC_000006.10:g.32045618C>T	NCBI36
NG_032652.1:g.16059C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337523.10:c.*15G>A MANE Select	ENSP00000337759.5:n.*15G>A
ENST00000337523.9:c.*15G>A	ENSP00000337759.5:n.*15G>A
ENST00000375349.7:c.*15G>A	ENSP00000364498.3:n.*15G>A
ENST00000375356.7:c.*15G>A	ENSP00000364505.3:n.*15G>A
ENST00000473976.1:n.1978G>A
ENST00000477826.5:n.2041G>A
ENST00000478221.5:n.1087G>A
ENST00000485557.5:n.1826G>A
ENST00000491327.5:n.1343G>A
ENST00000495340.5:c.539G>A
NM_005510.3:c.*15G>A	NP_005501.2:n.*15G>A
XM_006715005.2:c.*15G>A	XP_006715068.1:n.*15G>A
XM_006715007.2:c.*15G>A	XP_006715070.1:n.*15G>A
XR_926081.1:n.1679G>A
XR_926082.1:n.1706G>A
XM_006715005.3:c.*15G>A	XP_006715068.1:n.*15G>A
XM_017010329.1:c.*15G>A	XP_016865818.1:n.*15G>A
XR_002956262.1:n.1438G>A
XR_002956263.1:n.1604G>A
XR_002956264.1:n.1504G>A
XR_926082.2:n.1446G>A
NM_005510.4:c.*15G>A MANE Select	NP_005501.2:n.*15G>A
NM_001371205.1:c.*15G>A	NP_001358134.1:n.*15G>A
NM_001371206.1:c.*15G>A	NP_001358135.1:n.*15G>A