Canonical Allele Identifier: CA2172870372

Gene: CDAN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42731214C= , CM000677.2:g.42731214C=	GRCh38
NC_000015.9:g.43023412C= , CM000677.1:g.43023412C=	GRCh37
NC_000015.8:g.40810704C=	NCBI36
NG_012491.1:g.11006G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000356231.4:c.1857G= MANE Select	ENSP00000348564.3:p.Trp619=
ENST00000643434.1:c.*1035G=	ENSP00000494699.1:n.*1035G=
ENST00000356231.3:c.1857G=	ENSP00000348564.3:p.Trp619=
NM_138477.2:c.1857G=	NP_612486.2:p.Trp619=
XM_005254176.3:c.1860G=	XP_005254233.1:p.Trp620=
XM_011521270.1:c.1884G=	XP_011519572.1:p.Trp628=
XM_011521271.1:c.1881G=	XP_011519573.1:p.Trp627=
XM_011521272.1:c.1884G=	XP_011519574.1:p.Trp628=
XM_011521273.1:c.1884G=	XP_011519575.1:p.Trp628=
XM_011521274.1:c.849G=	XP_011519576.1:p.Trp283=
XM_011521275.1:c.1101G=	XP_011519577.1:p.Trp367=
XR_931757.1:n.1895G=
NM_138477.4:c.1857G= MANE Select	NP_612486.2:p.Trp619=
XM_005254176.5:c.1860G=	XP_005254233.1:p.Trp620=
XM_011521270.2:c.1884G=	XP_011519572.1:p.Trp628=
XM_011521271.2:c.1881G=	XP_011519573.1:p.Trp627=
XM_011521274.2:c.849G=	XP_011519576.1:p.Trp283=
XR_001751104.1:n.1914G=
XR_001751105.1:n.1914G=
XR_931757.2:n.1915G=