Canonical Allele Identifier: CA392042485

Gene: CDAN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42730692G>A , CM000677.2:g.42730692G>A	GRCh38
NC_000015.9:g.43022890G>A , CM000677.1:g.43022890G>A	GRCh37
NC_000015.8:g.40810182G>A	NCBI36
NG_012491.1:g.11528C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356231.4:c.2080C>T MANE Select	ENSP00000348564.3:p.Pro694Ser
ENST00000643434.1:c.*1258C>T	ENSP00000494699.1:n.*1258C>T
ENST00000356231.3:c.2080C>T	ENSP00000348564.3:p.Pro694Ser
ENST00000562465.5:c.73C>T	ENSP00000454246.1:p.Pro25Ser
NM_138477.2:c.2080C>T	NP_612486.2:p.Pro694Ser
XM_005254176.3:c.2083C>T	XP_005254233.1:p.Pro695Ser
XM_011521270.1:c.2107C>T	XP_011519572.1:p.Pro703Ser
XM_011521271.1:c.2104C>T	XP_011519573.1:p.Pro702Ser
XM_011521272.1:c.2107C>T	XP_011519574.1:p.Pro703Ser
XM_011521273.1:c.2107C>T	XP_011519575.1:p.Pro703Ser
XM_011521274.1:c.1072C>T	XP_011519576.1:p.Pro358Ser
XM_011521275.1:c.1324C>T	XP_011519577.1:p.Pro442Ser
XR_931757.1:n.2080C>T
NM_138477.4:c.2080C>T MANE Select	NP_612486.2:p.Pro694Ser
XM_005254176.5:c.2083C>T	XP_005254233.1:p.Pro695Ser
XM_011521270.2:c.2107C>T	XP_011519572.1:p.Pro703Ser
XM_011521271.2:c.2104C>T	XP_011519573.1:p.Pro702Ser
XM_011521274.2:c.1072C>T	XP_011519576.1:p.Pro358Ser
XR_001751104.1:n.2137C>T
XR_001751105.1:n.2137C>T
XR_931757.2:n.2100C>T