Canonical Allele Identifier: CA7515869

Gene: CDAN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42730964G>A , CM000677.2:g.42730964G>A	GRCh38
NC_000015.9:g.43023162G>A , CM000677.1:g.43023162G>A	GRCh37
NC_000015.8:g.40810454G>A	NCBI36
NG_012491.1:g.11256C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356231.4:c.1968C>T MANE Select	ENSP00000348564.3:p.Thr656=
ENST00000643434.1:c.*1146C>T	ENSP00000494699.1:n.*1146C>T
ENST00000356231.3:c.1968C>T	ENSP00000348564.3:p.Thr656=
NM_138477.2:c.1968C>T	NP_612486.2:p.Thr656=
XM_005254176.3:c.1971C>T	XP_005254233.1:p.Thr657=
XM_011521270.1:c.1995C>T	XP_011519572.1:p.Thr665=
XM_011521271.1:c.1992C>T	XP_011519573.1:p.Thr664=
XM_011521272.1:c.1995C>T	XP_011519574.1:p.Thr665=
XM_011521273.1:c.1995C>T	XP_011519575.1:p.Thr665=
XM_011521274.1:c.960C>T	XP_011519576.1:p.Thr320=
XM_011521275.1:c.1212C>T	XP_011519577.1:p.Thr404=
XR_931757.1:n.2006C>T
NM_138477.4:c.1968C>T MANE Select	NP_612486.2:p.Thr656=
XM_005254176.5:c.1971C>T	XP_005254233.1:p.Thr657=
XM_011521270.2:c.1995C>T	XP_011519572.1:p.Thr665=
XM_011521271.2:c.1992C>T	XP_011519573.1:p.Thr664=
XM_011521274.2:c.960C>T	XP_011519576.1:p.Thr320=
XR_001751104.1:n.2025C>T
XR_001751105.1:n.2025C>T
XR_931757.2:n.2026C>T