Canonical Allele Identifier: CA7515488

Gene: CDAN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42728721G>A , CM000677.2:g.42728721G>A	GRCh38
NC_000015.9:g.43020919G>A , CM000677.1:g.43020919G>A	GRCh37
NC_000015.8:g.40808211G>A	NCBI36
NG_012491.1:g.13499C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356231.4:c.2735C>T MANE Select	ENSP00000348564.3:p.Ala912Val
ENST00000643434.1:c.*1913C>T	ENSP00000494699.1:n.*1913C>T
ENST00000356231.3:c.2735C>T	ENSP00000348564.3:p.Ala912Val
ENST00000562465.5:c.728C>T	ENSP00000454246.1:p.Ala243Val
NM_138477.2:c.2735C>T	NP_612486.2:p.Ala912Val
XM_005254176.3:c.2738C>T	XP_005254233.1:p.Ala913Val
XM_011521270.1:c.2762C>T	XP_011519572.1:p.Ala921Val
XM_011521271.1:c.2759C>T	XP_011519573.1:p.Ala920Val
XM_011521272.1:c.2762C>T	XP_011519574.1:p.Ala921Val
XM_011521273.1:c.2762C>T	XP_011519575.1:p.Ala921Val
XM_011521274.1:c.1727C>T	XP_011519576.1:p.Ala576Val
XM_011521275.1:c.1979C>T	XP_011519577.1:p.Ala660Val
NM_138477.4:c.2735C>T MANE Select	NP_612486.2:p.Ala912Val
XM_005254176.5:c.2738C>T	XP_005254233.1:p.Ala913Val
XM_011521270.2:c.2762C>T	XP_011519572.1:p.Ala921Val
XM_011521271.2:c.2759C>T	XP_011519573.1:p.Ala920Val
XM_011521274.2:c.1727C>T	XP_011519576.1:p.Ala576Val
XR_001751104.1:n.2792C>T
XR_001751105.1:n.2792C>T