Canonical Allele Identifier: CA2172873843

Gene: CDAN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42736715G= , CM000677.2:g.42736715G=	GRCh38
NC_000015.9:g.43028913G= , CM000677.1:g.43028913G=	GRCh37
NC_000015.8:g.40816205G=	NCBI36
NG_012491.1:g.5505C=

Transcript Alleles

HGVS	Amino-acid Change
NM_138477.4:c.156C= MANE Select	NP_612486.2:p.Phe52=
ENST00000356231.4:c.156C= MANE Select	ENSP00000348564.3:p.Phe52=
NM_138477.2:c.156C=	NP_612486.2:p.Phe52=
ENST00000356231.3:c.156C=	ENSP00000348564.3:p.Phe52=
ENST00000563260.1:c.132C=	ENSP00000455536.1:p.Phe44=
ENST00000643434.1:c.90+298C=	ENSP00000494699.1:n.90+298C=
XM_005254176.3:c.156C=	XP_005254233.1:p.Phe52=
XM_005254176.5:c.156C=	XP_005254233.1:p.Phe52=
XM_011521270.1:c.180C=	XP_011519572.1:p.Phe60=
XM_011521270.2:c.180C=	XP_011519572.1:p.Phe60=
XM_011521271.1:c.180C=	XP_011519573.1:p.Phe60=
XM_011521271.2:c.180C=	XP_011519573.1:p.Phe60=
XM_011521272.1:c.180C=	XP_011519574.1:p.Phe60=
XM_011521273.1:c.180C=	XP_011519575.1:p.Phe60=
XM_011521275.1:c.-191+298C=	XP_011519577.1:n.-191+298C=
XR_001751104.1:n.210C=
XR_001751105.1:n.210C=
XR_931757.1:n.191C=
XR_931757.2:n.211C=