Canonical Allele Identifier: CA269909486

Gene: CDAN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42733700_42733703del , CM000677.2:g.42733700_42733703del	GRCh38
NC_000015.9:g.43025898_43025901del , CM000677.1:g.43025898_43025901del	GRCh37
NC_000015.8:g.40813190_40813193del	NCBI36
NG_012491.1:g.8521_8524del

Transcript Alleles

HGVS	Amino-acid Change
NM_138477.4:c.1367+239_1367+242del MANE Select	NP_612486.2:n.1367+239_1367+242del
ENST00000356231.4:c.1367+239_1367+242del MANE Select	ENSP00000348564.3:n.1367+239_1367+242del
NM_138477.2:c.1367+239_1367+242del	NP_612486.2:n.1367+239_1367+242del
ENST00000356231.3:c.1367+239_1367+242del	ENSP00000348564.3:n.1367+239_1367+242del
ENST00000643434.1:c.*545+239_*545+242del	ENSP00000494699.1:n.*545+239_*545+242del
XM_005254176.3:c.1370+239_1370+242del	XP_005254233.1:n.1370+239_1370+242del
XM_005254176.5:c.1370+239_1370+242del	XP_005254233.1:n.1370+239_1370+242del
XM_011521270.1:c.1394+239_1394+242del	XP_011519572.1:n.1394+239_1394+242del
XM_011521270.2:c.1394+239_1394+242del	XP_011519572.1:n.1394+239_1394+242del
XM_011521271.1:c.1391+239_1391+242del	XP_011519573.1:n.1391+239_1391+242del
XM_011521271.2:c.1391+239_1391+242del	XP_011519573.1:n.1391+239_1391+242del
XM_011521272.1:c.1394+239_1394+242del	XP_011519574.1:n.1394+239_1394+242del
XM_011521273.1:c.1394+239_1394+242del	XP_011519575.1:n.1394+239_1394+242del
XM_011521274.1:c.359+239_359+242del	XP_011519576.1:n.359+239_359+242del
XM_011521274.2:c.359+239_359+242del	XP_011519576.1:n.359+239_359+242del
XM_011521275.1:c.611+239_611+242del	XP_011519577.1:n.611+239_611+242del
XR_001751104.1:n.1424+239_1424+242del
XR_001751105.1:n.1424+239_1424+242del
XR_931757.1:n.1405+239_1405+242del
XR_931757.2:n.1425+239_1425+242del