Canonical Allele Identifier: CA392032733

Gene: CDAN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42727955C>G , CM000677.2:g.42727955C>G	GRCh38
NC_000015.9:g.43020153C>G , CM000677.1:g.43020153C>G	GRCh37
NC_000015.8:g.40807445C>G	NCBI36
NG_012491.1:g.14265G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_138477.4:c.2947G>C MANE Select	NP_612486.2:p.Ala983Pro
ENST00000356231.4:c.2947G>C MANE Select	ENSP00000348564.3:p.Ala983Pro
NM_138477.2:c.2947G>C	NP_612486.2:p.Ala983Pro
ENST00000356231.3:c.2947G>C	ENSP00000348564.3:p.Ala983Pro
ENST00000562465.5:c.940G>C	ENSP00000454246.1:p.Ala314Pro
ENST00000643434.1:c.*2125G>C	ENSP00000494699.1:n.*2125G>C
XM_005254176.3:c.2950G>C	XP_005254233.1:p.Ala984Pro
XM_005254176.5:c.2950G>C	XP_005254233.1:p.Ala984Pro
XM_011521270.1:c.2974G>C	XP_011519572.1:p.Ala992Pro
XM_011521270.2:c.2974G>C	XP_011519572.1:p.Ala992Pro
XM_011521271.1:c.2971G>C	XP_011519573.1:p.Ala991Pro
XM_011521271.2:c.2971G>C	XP_011519573.1:p.Ala991Pro
XM_011521272.1:c.2974G>C	XP_011519574.1:p.Ala992Pro
XM_011521273.1:c.2974G>C	XP_011519575.1:p.Ala992Pro
XM_011521274.1:c.1939G>C	XP_011519576.1:p.Ala647Pro
XM_011521274.2:c.1939G>C	XP_011519576.1:p.Ala647Pro
XM_011521275.1:c.2191G>C	XP_011519577.1:p.Ala731Pro
XR_001751104.1:n.3004G>C
XR_001751105.1:n.3004G>C