Canonical Allele Identifier: CA2172867525

Gene: CDAN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42726386T= , CM000677.2:g.42726386T=	GRCh38
NC_000015.9:g.43018584T= , CM000677.1:g.43018584T=	GRCh37
NC_000015.8:g.40805876T=	NCBI36
NG_012491.1:g.15834A=

Transcript Alleles

HGVS	Amino-acid Change
NM_138477.4:c.3128A= MANE Select	NP_612486.2:p.Asp1043=
ENST00000356231.4:c.3128A= MANE Select	ENSP00000348564.3:p.Asp1043=
NM_138477.2:c.3128A=	NP_612486.2:p.Asp1043=
ENST00000356231.3:c.3128A=	ENSP00000348564.3:p.Asp1043=
ENST00000562465.5:c.1074A=	ENSP00000454246.1:n.1074A=
ENST00000643434.1:c.*2259A=	ENSP00000494699.1:n.*2259A=
XM_005254176.3:c.3131A=	XP_005254233.1:p.Asp1044=
XM_005254176.5:c.3131A=	XP_005254233.1:p.Asp1044=
XM_011521270.1:c.3155A=	XP_011519572.1:p.Asp1052=
XM_011521270.2:c.3155A=	XP_011519572.1:p.Asp1052=
XM_011521271.1:c.3152A=	XP_011519573.1:p.Asp1051=
XM_011521271.2:c.3152A=	XP_011519573.1:p.Asp1051=
XM_011521272.1:c.3155A=	XP_011519574.1:p.Asp1052=
XM_011521273.1:c.*30A=	XP_011519575.1:n.*30A=
XM_011521274.1:c.2120A=	XP_011519576.1:p.Asp707=
XM_011521274.2:c.2120A=	XP_011519576.1:p.Asp707=
XM_011521275.1:c.2372A=	XP_011519577.1:p.Asp791=
XR_001751104.1:n.3185A=
XR_001751105.1:n.3138A=