Canonical Allele Identifier: CA2575698522

Gene: CDAN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42731190T>C , CM000677.2:g.42731190T>C	GRCh38
NC_000015.9:g.43023388T>C , CM000677.1:g.43023388T>C	GRCh37
NC_000015.8:g.40810680T>C	NCBI36
NG_012491.1:g.11030A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356231.4:c.1860+21A>G MANE Select	ENSP00000348564.3:n.1860+21A>G
ENST00000643434.1:c.*1038+21A>G	ENSP00000494699.1:n.*1038+21A>G
ENST00000356231.3:c.1860+21A>G	ENSP00000348564.3:n.1860+21A>G
NM_138477.2:c.1860+21A>G	NP_612486.2:n.1860+21A>G
XM_005254176.3:c.1863+21A>G	XP_005254233.1:n.1863+21A>G
XM_011521270.1:c.1887+21A>G	XP_011519572.1:n.1887+21A>G
XM_011521271.1:c.1884+21A>G	XP_011519573.1:n.1884+21A>G
XM_011521272.1:c.1887+21A>G	XP_011519574.1:n.1887+21A>G
XM_011521273.1:c.1887+21A>G	XP_011519575.1:n.1887+21A>G
XM_011521274.1:c.852+21A>G	XP_011519576.1:n.852+21A>G
XM_011521275.1:c.1104+21A>G	XP_011519577.1:n.1104+21A>G
XR_931757.1:n.1898+21A>G
NM_138477.4:c.1860+21A>G MANE Select	NP_612486.2:n.1860+21A>G
XM_005254176.5:c.1863+21A>G	XP_005254233.1:n.1863+21A>G
XM_011521270.2:c.1887+21A>G	XP_011519572.1:n.1887+21A>G
XM_011521271.2:c.1884+21A>G	XP_011519573.1:n.1884+21A>G
XM_011521274.2:c.852+21A>G	XP_011519576.1:n.852+21A>G
XR_001751104.1:n.1917+21A>G
XR_001751105.1:n.1917+21A>G
XR_931757.2:n.1918+21A>G