Canonical Allele Identifier: CA2172870096

Gene: CDAN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42730634T= , CM000677.2:g.42730634T=	GRCh38
NC_000015.9:g.43022832T= , CM000677.1:g.43022832T=	GRCh37
NC_000015.8:g.40810124T=	NCBI36
NG_012491.1:g.11586A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000356231.4:c.2138A= MANE Select	ENSP00000348564.3:p.Tyr713=
ENST00000643434.1:c.*1316A=	ENSP00000494699.1:n.*1316A=
ENST00000356231.3:c.2138A=	ENSP00000348564.3:p.Tyr713=
ENST00000562465.5:c.131A=	ENSP00000454246.1:p.Tyr44=
NM_138477.2:c.2138A=	NP_612486.2:p.Tyr713=
XM_005254176.3:c.2141A=	XP_005254233.1:p.Tyr714=
XM_011521270.1:c.2165A=	XP_011519572.1:p.Tyr722=
XM_011521271.1:c.2162A=	XP_011519573.1:p.Tyr721=
XM_011521272.1:c.2165A=	XP_011519574.1:p.Tyr722=
XM_011521273.1:c.2165A=	XP_011519575.1:p.Tyr722=
XM_011521274.1:c.1130A=	XP_011519576.1:p.Tyr377=
XM_011521275.1:c.1382A=	XP_011519577.1:p.Tyr461=
XR_931757.1:n.2138A=
NM_138477.4:c.2138A= MANE Select	NP_612486.2:p.Tyr713=
XM_005254176.5:c.2141A=	XP_005254233.1:p.Tyr714=
XM_011521270.2:c.2165A=	XP_011519572.1:p.Tyr722=
XM_011521271.2:c.2162A=	XP_011519573.1:p.Tyr721=
XM_011521274.2:c.1130A=	XP_011519576.1:p.Tyr377=
XR_001751104.1:n.2195A=
XR_001751105.1:n.2195A=
XR_931757.2:n.2158A=