Canonical Allele Identifier: CA392044399

Gene: CDAN1

Linked Data

• MyVariant Identifiers: chr15:g.43023421G>T (hg19) ; chr15:g.42731223G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42731223G>T , CM000677.2:g.42731223G>T	GRCh38
NC_000015.9:g.43023421G>T , CM000677.1:g.43023421G>T	GRCh37
NC_000015.8:g.40810713G>T	NCBI36
NG_012491.1:g.10997C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356231.4:c.1848C>A MANE Select	ENSP00000348564.3:p.Asp616Glu
ENST00000643434.1:c.*1026C>A	ENSP00000494699.1:n.*1026C>A
ENST00000356231.3:c.1848C>A	ENSP00000348564.3:p.Asp616Glu
NM_138477.2:c.1848C>A	NP_612486.2:p.Asp616Glu
XM_005254176.3:c.1851C>A	XP_005254233.1:p.Asp617Glu
XM_011521270.1:c.1875C>A	XP_011519572.1:p.Asp625Glu
XM_011521271.1:c.1872C>A	XP_011519573.1:p.Asp624Glu
XM_011521272.1:c.1875C>A	XP_011519574.1:p.Asp625Glu
XM_011521273.1:c.1875C>A	XP_011519575.1:p.Asp625Glu
XM_011521274.1:c.840C>A	XP_011519576.1:p.Asp280Glu
XM_011521275.1:c.1092C>A	XP_011519577.1:p.Asp364Glu
XR_931757.1:n.1886C>A
NM_138477.4:c.1848C>A MANE Select	NP_612486.2:p.Asp616Glu
XM_005254176.5:c.1851C>A	XP_005254233.1:p.Asp617Glu
XM_011521270.2:c.1875C>A	XP_011519572.1:p.Asp625Glu
XM_011521271.2:c.1872C>A	XP_011519573.1:p.Asp624Glu
XM_011521274.2:c.840C>A	XP_011519576.1:p.Asp280Glu
XR_001751104.1:n.1905C>A
XR_001751105.1:n.1905C>A
XR_931757.2:n.1906C>A