Canonical Allele Identifier: CA7515432

Gene: CDAN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42728210C>T , CM000677.2:g.42728210C>T	GRCh38
NC_000015.9:g.43020408C>T , CM000677.1:g.43020408C>T	GRCh37
NC_000015.8:g.40807700C>T	NCBI36
NG_012491.1:g.14010G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356231.4:c.2862G>A MANE Select	ENSP00000348564.3:p.Pro954=
ENST00000643434.1:c.*2040G>A	ENSP00000494699.1:n.*2040G>A
ENST00000356231.3:c.2862G>A	ENSP00000348564.3:p.Pro954=
ENST00000562465.5:c.855G>A	ENSP00000454246.1:p.Pro285=
NM_138477.2:c.2862G>A	NP_612486.2:p.Pro954=
XM_005254176.3:c.2865G>A	XP_005254233.1:p.Pro955=
XM_011521270.1:c.2889G>A	XP_011519572.1:p.Pro963=
XM_011521271.1:c.2886G>A	XP_011519573.1:p.Pro962=
XM_011521272.1:c.2889G>A	XP_011519574.1:p.Pro963=
XM_011521273.1:c.2889G>A	XP_011519575.1:p.Pro963=
XM_011521274.1:c.1854G>A	XP_011519576.1:p.Pro618=
XM_011521275.1:c.2106G>A	XP_011519577.1:p.Pro702=
NM_138477.4:c.2862G>A MANE Select	NP_612486.2:p.Pro954=
XM_005254176.5:c.2865G>A	XP_005254233.1:p.Pro955=
XM_011521270.2:c.2889G>A	XP_011519572.1:p.Pro963=
XM_011521271.2:c.2886G>A	XP_011519573.1:p.Pro962=
XM_011521274.2:c.1854G>A	XP_011519576.1:p.Pro618=
XR_001751104.1:n.2919G>A
XR_001751105.1:n.2919G>A