Canonical Allele Identifier: CA7516261

Gene: CDAN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42735637G>T , CM000677.2:g.42735637G>T	GRCh38
NC_000015.9:g.43027835G>T , CM000677.1:g.43027835G>T	GRCh37
NC_000015.8:g.40815127G>T	NCBI36
NG_012491.1:g.6583C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356231.4:c.816C>A MANE Select	ENSP00000348564.3:p.Thr272=
ENST00000643434.1:c.*115C>A	ENSP00000494699.1:n.*115C>A
ENST00000356231.3:c.816C>A	ENSP00000348564.3:p.Thr272=
NM_138477.2:c.816C>A	NP_612486.2:p.Thr272=
XM_005254176.3:c.819C>A	XP_005254233.1:p.Thr273=
XM_011521270.1:c.843C>A	XP_011519572.1:p.Thr281=
XM_011521271.1:c.840C>A	XP_011519573.1:p.Thr280=
XM_011521272.1:c.843C>A	XP_011519574.1:p.Thr281=
XM_011521273.1:c.843C>A	XP_011519575.1:p.Thr281=
XM_011521275.1:c.60C>A	XP_011519577.1:p.Thr20=
XR_931757.1:n.854C>A
NM_138477.4:c.816C>A MANE Select	NP_612486.2:p.Thr272=
XM_005254176.5:c.819C>A	XP_005254233.1:p.Thr273=
XM_011521270.2:c.843C>A	XP_011519572.1:p.Thr281=
XM_011521271.2:c.840C>A	XP_011519573.1:p.Thr280=
XR_001751104.1:n.873C>A
XR_001751105.1:n.873C>A
XR_931757.2:n.874C>A