Canonical Allele Identifier: CA392042159
Gene: CDAN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.42730633G>C , CM000677.2:g.42730633G>C GRCh38
NC_000015.9:g.43022831G>C , CM000677.1:g.43022831G>C GRCh37
NC_000015.8:g.40810123G>C NCBI36
NG_012491.1:g.11587C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000356231.4:c.2139C>G MANE Select ENSP00000348564.3:p.Tyr713Ter
ENST00000643434.1:c.*1317C>G ENSP00000494699.1:n.*1317C>G
ENST00000356231.3:c.2139C>G ENSP00000348564.3:p.Tyr713Ter
ENST00000562465.5:c.132C>G ENSP00000454246.1:p.Tyr44Ter
NM_138477.2:c.2139C>G NP_612486.2:p.Tyr713Ter
XM_005254176.3:c.2142C>G XP_005254233.1:p.Tyr714Ter
XM_011521270.1:c.2166C>G XP_011519572.1:p.Tyr722Ter
XM_011521271.1:c.2163C>G XP_011519573.1:p.Tyr721Ter
XM_011521272.1:c.2166C>G XP_011519574.1:p.Tyr722Ter
XM_011521273.1:c.2166C>G XP_011519575.1:p.Tyr722Ter
XM_011521274.1:c.1131C>G XP_011519576.1:p.Tyr377Ter
XM_011521275.1:c.1383C>G XP_011519577.1:p.Tyr461Ter
XR_931757.1:n.2139C>G
NM_138477.4:c.2139C>G MANE Select NP_612486.2:p.Tyr713Ter
XM_005254176.5:c.2142C>G XP_005254233.1:p.Tyr714Ter
XM_011521270.2:c.2166C>G XP_011519572.1:p.Tyr722Ter
XM_011521271.2:c.2163C>G XP_011519573.1:p.Tyr721Ter
XM_011521274.2:c.1131C>G XP_011519576.1:p.Tyr377Ter
XR_001751104.1:n.2196C>G
XR_001751105.1:n.2196C>G
XR_931757.2:n.2159C>G