Canonical Allele Identifier: CA7515112
Gene: CDAN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.42725221G>T , CM000677.2:g.42725221G>T GRCh38
NC_000015.9:g.43017419G>T , CM000677.1:g.43017419G>T GRCh37
NC_000015.8:g.40804711G>T NCBI36
NG_012491.1:g.16999C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000356231.4:c.3481C>A MANE Select ENSP00000348564.3:p.Leu1161Met
ENST00000643434.1:c.*2548C>A ENSP00000494699.1:n.*2548C>A
ENST00000356231.3:c.3481C>A ENSP00000348564.3:p.Leu1161Met
ENST00000562465.5:c.1427C>A ENSP00000454246.1:n.1427C>A
ENST00000563604.1:n.417C>A
ENST00000565930.1:n.82C>A
NM_138477.2:c.3481C>A NP_612486.2:p.Leu1161Met
XM_005254176.3:c.3484C>A XP_005254233.1:p.Leu1162Met
XM_011521270.1:c.3508C>A XP_011519572.1:p.Leu1170Met
XM_011521271.1:c.3505C>A XP_011519573.1:p.Leu1169Met
XM_011521274.1:c.2473C>A XP_011519576.1:p.Leu825Met
XM_011521275.1:c.2725C>A XP_011519577.1:p.Leu909Met
NM_138477.4:c.3481C>A MANE Select NP_612486.2:p.Leu1161Met
XM_005254176.5:c.3484C>A XP_005254233.1:p.Leu1162Met
XM_011521270.2:c.3508C>A XP_011519572.1:p.Leu1170Met
XM_011521271.2:c.3505C>A XP_011519573.1:p.Leu1169Met
XM_011521274.2:c.2473C>A XP_011519576.1:p.Leu825Met
XR_001751104.1:n.3474C>A
XR_001751105.1:n.3491C>A