Canonical Allele Identifier: CA14078504

Gene: CDAN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42730492C>A , CM000677.2:g.42730492C>A	GRCh38
NC_000015.9:g.43022690C>A , CM000677.1:g.43022690C>A	GRCh37
NC_000015.8:g.40809982C>A	NCBI36
NG_012491.1:g.11728G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_138477.4:c.2174+106G>T MANE Select	NP_612486.2:n.2174+106G>T
ENST00000356231.4:c.2174+106G>T MANE Select	ENSP00000348564.3:n.2174+106G>T
NM_138477.2:c.2174+106G>T	NP_612486.2:n.2174+106G>T
ENST00000356231.3:c.2174+106G>T	ENSP00000348564.3:n.2174+106G>T
ENST00000562465.5:c.167+106G>T	ENSP00000454246.1:n.167+106G>T
ENST00000643434.1:c.*1352+106G>T	ENSP00000494699.1:n.*1352+106G>T
XM_005254176.3:c.2177+106G>T	XP_005254233.1:n.2177+106G>T
XM_005254176.5:c.2177+106G>T	XP_005254233.1:n.2177+106G>T
XM_011521270.1:c.2201+106G>T	XP_011519572.1:n.2201+106G>T
XM_011521270.2:c.2201+106G>T	XP_011519572.1:n.2201+106G>T
XM_011521271.1:c.2198+106G>T	XP_011519573.1:n.2198+106G>T
XM_011521271.2:c.2198+106G>T	XP_011519573.1:n.2198+106G>T
XM_011521272.1:c.2201+106G>T	XP_011519574.1:n.2201+106G>T
XM_011521273.1:c.2201+106G>T	XP_011519575.1:n.2201+106G>T
XM_011521274.1:c.1166+106G>T	XP_011519576.1:n.1166+106G>T
XM_011521274.2:c.1166+106G>T	XP_011519576.1:n.1166+106G>T
XM_011521275.1:c.1418+106G>T	XP_011519577.1:n.1418+106G>T
XR_001751104.1:n.2231+106G>T
XR_001751105.1:n.2231+106G>T
XR_931757.1:n.2174+106G>T
XR_931757.2:n.2194+106G>T