Canonical Allele Identifier: CA2172869188

Gene: CDAN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42729071A= , CM000677.2:g.42729071A=	GRCh38
NC_000015.9:g.43021269A= , CM000677.1:g.43021269A=	GRCh37
NC_000015.8:g.40808561A=	NCBI36
NG_012491.1:g.13149T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000356231.4:c.2597T= MANE Select	ENSP00000348564.3:p.Val866=
ENST00000643434.1:c.*1775T=	ENSP00000494699.1:n.*1775T=
ENST00000356231.3:c.2597T=	ENSP00000348564.3:p.Val866=
ENST00000562465.5:c.590T=	ENSP00000454246.1:p.Val197=
NM_138477.2:c.2597T=	NP_612486.2:p.Val866=
XM_005254176.3:c.2600T=	XP_005254233.1:p.Val867=
XM_011521270.1:c.2624T=	XP_011519572.1:p.Val875=
XM_011521271.1:c.2621T=	XP_011519573.1:p.Val874=
XM_011521272.1:c.2624T=	XP_011519574.1:p.Val875=
XM_011521273.1:c.2624T=	XP_011519575.1:p.Val875=
XM_011521274.1:c.1589T=	XP_011519576.1:p.Val530=
XM_011521275.1:c.1841T=	XP_011519577.1:p.Val614=
NM_138477.4:c.2597T= MANE Select	NP_612486.2:p.Val866=
XM_005254176.5:c.2600T=	XP_005254233.1:p.Val867=
XM_011521270.2:c.2624T=	XP_011519572.1:p.Val875=
XM_011521271.2:c.2621T=	XP_011519573.1:p.Val874=
XM_011521274.2:c.1589T=	XP_011519576.1:p.Val530=
XR_001751104.1:n.2654T=
XR_001751105.1:n.2654T=