Canonical Allele Identifier: CA7515323

Gene: CDAN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42727671C>T , CM000677.2:g.42727671C>T	GRCh38
NC_000015.9:g.43019869C>T , CM000677.1:g.43019869C>T	GRCh37
NC_000015.8:g.40807161C>T	NCBI36
NG_012491.1:g.14549G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_138477.4:c.3046G>A MANE Select	NP_612486.2:p.Ala1016Thr
ENST00000356231.4:c.3046G>A MANE Select	ENSP00000348564.3:p.Ala1016Thr
NM_138477.2:c.3046G>A	NP_612486.2:p.Ala1016Thr
ENST00000356231.3:c.3046G>A	ENSP00000348564.3:p.Ala1016Thr
ENST00000562465.5:c.1039G>A	ENSP00000454246.1:p.Ala347Thr
ENST00000643434.1:c.*2224G>A	ENSP00000494699.1:n.*2224G>A
XM_005254176.3:c.3049G>A	XP_005254233.1:p.Ala1017Thr
XM_005254176.5:c.3049G>A	XP_005254233.1:p.Ala1017Thr
XM_011521270.1:c.3073G>A	XP_011519572.1:p.Ala1025Thr
XM_011521270.2:c.3073G>A	XP_011519572.1:p.Ala1025Thr
XM_011521271.1:c.3070G>A	XP_011519573.1:p.Ala1024Thr
XM_011521271.2:c.3070G>A	XP_011519573.1:p.Ala1024Thr
XM_011521272.1:c.3073G>A	XP_011519574.1:p.Ala1025Thr
XM_011521273.1:c.3073G>A	XP_011519575.1:p.Ala1025Thr
XM_011521274.1:c.2038G>A	XP_011519576.1:p.Ala680Thr
XM_011521274.2:c.2038G>A	XP_011519576.1:p.Ala680Thr
XM_011521275.1:c.2290G>A	XP_011519577.1:p.Ala764Thr
XR_001751104.1:n.3103G>A
XR_001751105.1:n.3103G>A