Canonical Allele Identifier: CA489894788

Gene: CDAN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42729331C>T , CM000677.2:g.42729331C>T	GRCh38
NC_000015.9:g.43021529C>T , CM000677.1:g.43021529C>T	GRCh37
NC_000015.8:g.40808821C>T	NCBI36
NG_012491.1:g.12889G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356231.4:c.2439G>A MANE Select	ENSP00000348564.3:p.Val813=
ENST00000643434.1:c.*1617G>A	ENSP00000494699.1:n.*1617G>A
ENST00000356231.3:c.2439G>A	ENSP00000348564.3:p.Val813=
ENST00000562465.5:c.432G>A	ENSP00000454246.1:p.Val144=
NM_138477.2:c.2439G>A	NP_612486.2:p.Val813=
XM_005254176.3:c.2442G>A	XP_005254233.1:p.Val814=
XM_011521270.1:c.2466G>A	XP_011519572.1:p.Val822=
XM_011521271.1:c.2463G>A	XP_011519573.1:p.Val821=
XM_011521272.1:c.2466G>A	XP_011519574.1:p.Val822=
XM_011521273.1:c.2466G>A	XP_011519575.1:p.Val822=
XM_011521274.1:c.1431G>A	XP_011519576.1:p.Val477=
XM_011521275.1:c.1683G>A	XP_011519577.1:p.Val561=
NM_138477.4:c.2439G>A MANE Select	NP_612486.2:p.Val813=
XM_005254176.5:c.2442G>A	XP_005254233.1:p.Val814=
XM_011521270.2:c.2466G>A	XP_011519572.1:p.Val822=
XM_011521271.2:c.2463G>A	XP_011519573.1:p.Val821=
XM_011521274.2:c.1431G>A	XP_011519576.1:p.Val477=
XR_001751104.1:n.2496G>A
XR_001751105.1:n.2496G>A