Canonical Allele Identifier: CA363492931

Gene: DXO

Linked Data

• MyVariant Identifiers: chr6:g.31937668G>C (hg19) ; chr6:g.31969891G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31969891G>C , CM000668.2:g.31969891G>C	GRCh38
NC_000006.11:g.31937668G>C , CM000668.1:g.31937668G>C	GRCh37
NC_000006.10:g.32045647G>C	NCBI36
NG_032652.1:g.16088G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337523.10:c.1177C>G MANE Select	ENSP00000337759.5:p.Pro393Ala
ENST00000337523.9:c.1177C>G	ENSP00000337759.5:p.Pro393Ala
ENST00000375349.7:c.1177C>G	ENSP00000364498.3:p.Pro393Ala
ENST00000375356.7:c.1177C>G	ENSP00000364505.3:p.Pro393Ala
ENST00000473976.1:n.1949C>G
ENST00000477826.5:n.2012C>G
ENST00000478221.5:n.1058C>G
ENST00000485557.5:n.1797C>G
ENST00000491327.5:n.1314C>G
ENST00000495340.5:c.510C>G
ENST00000498357.1:n.1621C>G
NM_005510.3:c.1177C>G	NP_005501.2:p.Pro393Ala
XM_006715005.2:c.1177C>G	XP_006715068.1:p.Pro393Ala
XM_006715007.2:c.625C>G	XP_006715070.1:p.Pro209Ala
XR_926081.1:n.1650C>G
XR_926082.1:n.1677C>G
XM_006715005.3:c.1177C>G	XP_006715068.1:p.Pro393Ala
XM_017010329.1:c.625C>G	XP_016865818.1:p.Pro209Ala
XR_002956262.1:n.1409C>G
XR_002956263.1:n.1575C>G
XR_002956264.1:n.1475C>G
XR_926082.2:n.1417C>G
NM_005510.4:c.1177C>G MANE Select	NP_005501.2:p.Pro393Ala
NM_001371205.1:c.625C>G	NP_001358134.1:p.Pro209Ala
NM_001371206.1:c.625C>G	NP_001358135.1:p.Pro209Ala