Canonical Allele Identifier: CA392044953

Gene: CDAN1

Linked Data

• MyVariant Identifiers: chr15:g.43023480C>T (hg19) ; chr15:g.42731282C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42731282C>T , CM000677.2:g.42731282C>T	GRCh38
NC_000015.9:g.43023480C>T , CM000677.1:g.43023480C>T	GRCh37
NC_000015.8:g.40810772C>T	NCBI36
NG_012491.1:g.10938G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000356231.4:c.1789G>A MANE Select	ENSP00000348564.3:p.Glu597Lys
ENST00000643434.1:c.*967G>A	ENSP00000494699.1:n.*967G>A
ENST00000356231.3:c.1789G>A	ENSP00000348564.3:p.Glu597Lys
NM_138477.2:c.1789G>A	NP_612486.2:p.Glu597Lys
XM_005254176.3:c.1792G>A	XP_005254233.1:p.Glu598Lys
XM_011521270.1:c.1816G>A	XP_011519572.1:p.Glu606Lys
XM_011521271.1:c.1813G>A	XP_011519573.1:p.Glu605Lys
XM_011521272.1:c.1816G>A	XP_011519574.1:p.Glu606Lys
XM_011521273.1:c.1816G>A	XP_011519575.1:p.Glu606Lys
XM_011521274.1:c.781G>A	XP_011519576.1:p.Glu261Lys
XM_011521275.1:c.1033G>A	XP_011519577.1:p.Glu345Lys
XR_931757.1:n.1827G>A
NM_138477.4:c.1789G>A MANE Select	NP_612486.2:p.Glu597Lys
XM_005254176.5:c.1792G>A	XP_005254233.1:p.Glu598Lys
XM_011521270.2:c.1816G>A	XP_011519572.1:p.Glu606Lys
XM_011521271.2:c.1813G>A	XP_011519573.1:p.Glu605Lys
XM_011521274.2:c.781G>A	XP_011519576.1:p.Glu261Lys
XR_001751104.1:n.1846G>A
XR_001751105.1:n.1846G>A
XR_931757.2:n.1847G>A