Canonical Allele Identifier: CA2628073980
Gene: CDAN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.42731471_42731472insTTT , CM000677.2:g.42731471_42731472insTTT GRCh38
NC_000015.9:g.43023669_43023670insTTT , CM000677.1:g.43023669_43023670insTTT GRCh37
NC_000015.8:g.40810961_40810962insTTT NCBI36
NG_012491.1:g.10748_10749insAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000356231.4:c.1740-141_1740-140insAAA MANE Select ENSP00000348564.3:n.1740-141_1740-140insAAA
ENST00000643434.1:c.*918-141_*918-140insAAA ENSP00000494699.1:n.*918-141_*918-140insAAA
ENST00000356231.3:c.1740-141_1740-140insAAA ENSP00000348564.3:n.1740-141_1740-140insAAA
NM_138477.2:c.1740-141_1740-140insAAA NP_612486.2:n.1740-141_1740-140insAAA
XM_005254176.3:c.1743-141_1743-140insAAA XP_005254233.1:n.1743-141_1743-140insAAA
XM_011521270.1:c.1767-141_1767-140insAAA XP_011519572.1:n.1767-141_1767-140insAAA
XM_011521271.1:c.1764-141_1764-140insAAA XP_011519573.1:n.1764-141_1764-140insAAA
XM_011521272.1:c.1767-141_1767-140insAAA XP_011519574.1:n.1767-141_1767-140insAAA
XM_011521273.1:c.1767-141_1767-140insAAA XP_011519575.1:n.1767-141_1767-140insAAA
XM_011521274.1:c.732-141_732-140insAAA XP_011519576.1:n.732-141_732-140insAAA
XM_011521275.1:c.984-141_984-140insAAA XP_011519577.1:n.984-141_984-140insAAA
XR_931757.1:n.1778-141_1778-140insAAA
NM_138477.4:c.1740-141_1740-140insAAA MANE Select NP_612486.2:n.1740-141_1740-140insAAA
XM_005254176.5:c.1743-141_1743-140insAAA XP_005254233.1:n.1743-141_1743-140insAAA
XM_011521270.2:c.1767-141_1767-140insAAA XP_011519572.1:n.1767-141_1767-140insAAA
XM_011521271.2:c.1764-141_1764-140insAAA XP_011519573.1:n.1764-141_1764-140insAAA
XM_011521274.2:c.732-141_732-140insAAA XP_011519576.1:n.732-141_732-140insAAA
XR_001751104.1:n.1797-141_1797-140insAAA
XR_001751105.1:n.1797-141_1797-140insAAA
XR_931757.2:n.1798-141_1798-140insAAA