Canonical Allele Identifier: CA392035510

Gene: CDAN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42728680C>G , CM000677.2:g.42728680C>G	GRCh38
NC_000015.9:g.43020878C>G , CM000677.1:g.43020878C>G	GRCh37
NC_000015.8:g.40808170C>G	NCBI36
NG_012491.1:g.13540G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356231.4:c.2776G>C MANE Select	ENSP00000348564.3:p.Gly926Arg
ENST00000643434.1:c.*1954G>C	ENSP00000494699.1:n.*1954G>C
ENST00000356231.3:c.2776G>C	ENSP00000348564.3:p.Gly926Arg
ENST00000562465.5:c.769G>C	ENSP00000454246.1:p.Gly257Arg
NM_138477.2:c.2776G>C	NP_612486.2:p.Gly926Arg
XM_005254176.3:c.2779G>C	XP_005254233.1:p.Gly927Arg
XM_011521270.1:c.2803G>C	XP_011519572.1:p.Gly935Arg
XM_011521271.1:c.2800G>C	XP_011519573.1:p.Gly934Arg
XM_011521272.1:c.2803G>C	XP_011519574.1:p.Gly935Arg
XM_011521273.1:c.2803G>C	XP_011519575.1:p.Gly935Arg
XM_011521274.1:c.1768G>C	XP_011519576.1:p.Gly590Arg
XM_011521275.1:c.2020G>C	XP_011519577.1:p.Gly674Arg
NM_138477.4:c.2776G>C MANE Select	NP_612486.2:p.Gly926Arg
XM_005254176.5:c.2779G>C	XP_005254233.1:p.Gly927Arg
XM_011521270.2:c.2803G>C	XP_011519572.1:p.Gly935Arg
XM_011521271.2:c.2800G>C	XP_011519573.1:p.Gly934Arg
XM_011521274.2:c.1768G>C	XP_011519576.1:p.Gly590Arg
XR_001751104.1:n.2833G>C
XR_001751105.1:n.2833G>C