Canonical Allele Identifier: CA489894660

Gene: CDAN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42728690C>A , CM000677.2:g.42728690C>A	GRCh38
NC_000015.9:g.43020888C>A , CM000677.1:g.43020888C>A	GRCh37
NC_000015.8:g.40808180C>A	NCBI36
NG_012491.1:g.13530G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_138477.4:c.2766G>T MANE Select	NP_612486.2:p.Leu922=
ENST00000356231.4:c.2766G>T MANE Select	ENSP00000348564.3:p.Leu922=
NM_138477.2:c.2766G>T	NP_612486.2:p.Leu922=
ENST00000356231.3:c.2766G>T	ENSP00000348564.3:p.Leu922=
ENST00000562465.5:c.759G>T	ENSP00000454246.1:p.Leu253=
ENST00000643434.1:c.*1944G>T	ENSP00000494699.1:n.*1944G>T
XM_005254176.3:c.2769G>T	XP_005254233.1:p.Leu923=
XM_005254176.5:c.2769G>T	XP_005254233.1:p.Leu923=
XM_011521270.1:c.2793G>T	XP_011519572.1:p.Leu931=
XM_011521270.2:c.2793G>T	XP_011519572.1:p.Leu931=
XM_011521271.1:c.2790G>T	XP_011519573.1:p.Leu930=
XM_011521271.2:c.2790G>T	XP_011519573.1:p.Leu930=
XM_011521272.1:c.2793G>T	XP_011519574.1:p.Leu931=
XM_011521273.1:c.2793G>T	XP_011519575.1:p.Leu931=
XM_011521274.1:c.1758G>T	XP_011519576.1:p.Leu586=
XM_011521274.2:c.1758G>T	XP_011519576.1:p.Leu586=
XM_011521275.1:c.2010G>T	XP_011519577.1:p.Leu670=
XR_001751104.1:n.2823G>T
XR_001751105.1:n.2823G>T