Canonical Allele Identifier: CA269902318
Community Standard Title: NM_138477.4(CDAN1):c.2805-129G>A
Gene: CDAN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.42728396C>T , CM000677.2:g.42728396C>T GRCh38
NC_000015.9:g.43020594C>T , CM000677.1:g.43020594C>T GRCh37
NC_000015.8:g.40807886C>T NCBI36
NG_012491.1:g.13824G>A

Transcript Alleles

HGVS Amino-acid Change
NM_138477.4:c.2805-129G>A MANE Select NP_612486.2:n.2805-129G>A
ENST00000356231.4:c.2805-129G>A MANE Select ENSP00000348564.3:n.2805-129G>A
NM_138477.2:c.2805-129G>A NP_612486.2:n.2805-129G>A
ENST00000356231.3:c.2805-129G>A ENSP00000348564.3:n.2805-129G>A
ENST00000562465.5:c.798-129G>A ENSP00000454246.1:n.798-129G>A
ENST00000643434.1:c.*1983-129G>A ENSP00000494699.1:n.*1983-129G>A
XM_005254176.3:c.2808-129G>A XP_005254233.1:n.2808-129G>A
XM_005254176.5:c.2808-129G>A XP_005254233.1:n.2808-129G>A
XM_011521270.1:c.2832-129G>A XP_011519572.1:n.2832-129G>A
XM_011521270.2:c.2832-129G>A XP_011519572.1:n.2832-129G>A
XM_011521271.1:c.2829-129G>A XP_011519573.1:n.2829-129G>A
XM_011521271.2:c.2829-129G>A XP_011519573.1:n.2829-129G>A
XM_011521272.1:c.2832-129G>A XP_011519574.1:n.2832-129G>A
XM_011521273.1:c.2832-129G>A XP_011519575.1:n.2832-129G>A
XM_011521274.1:c.1797-129G>A XP_011519576.1:n.1797-129G>A
XM_011521274.2:c.1797-129G>A XP_011519576.1:n.1797-129G>A
XM_011521275.1:c.2049-129G>A XP_011519577.1:n.2049-129G>A
XR_001751104.1:n.2862-129G>A
XR_001751105.1:n.2862-129G>A