Canonical Allele Identifier: CA392042180
Gene: CDAN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.42730637T>A , CM000677.2:g.42730637T>A GRCh38
NC_000015.9:g.43022835T>A , CM000677.1:g.43022835T>A GRCh37
NC_000015.8:g.40810127T>A NCBI36
NG_012491.1:g.11583A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000356231.4:c.2135A>T MANE Select ENSP00000348564.3:p.Tyr712Phe
ENST00000643434.1:c.*1313A>T ENSP00000494699.1:n.*1313A>T
ENST00000356231.3:c.2135A>T ENSP00000348564.3:p.Tyr712Phe
ENST00000562465.5:c.128A>T ENSP00000454246.1:p.Tyr43Phe
NM_138477.2:c.2135A>T NP_612486.2:p.Tyr712Phe
XM_005254176.3:c.2138A>T XP_005254233.1:p.Tyr713Phe
XM_011521270.1:c.2162A>T XP_011519572.1:p.Tyr721Phe
XM_011521271.1:c.2159A>T XP_011519573.1:p.Tyr720Phe
XM_011521272.1:c.2162A>T XP_011519574.1:p.Tyr721Phe
XM_011521273.1:c.2162A>T XP_011519575.1:p.Tyr721Phe
XM_011521274.1:c.1127A>T XP_011519576.1:p.Tyr376Phe
XM_011521275.1:c.1379A>T XP_011519577.1:p.Tyr460Phe
XR_931757.1:n.2135A>T
NM_138477.4:c.2135A>T MANE Select NP_612486.2:p.Tyr712Phe
XM_005254176.5:c.2138A>T XP_005254233.1:p.Tyr713Phe
XM_011521270.2:c.2162A>T XP_011519572.1:p.Tyr721Phe
XM_011521271.2:c.2159A>T XP_011519573.1:p.Tyr720Phe
XM_011521274.2:c.1127A>T XP_011519576.1:p.Tyr376Phe
XR_001751104.1:n.2192A>T
XR_001751105.1:n.2192A>T
XR_931757.2:n.2155A>T