Canonical Allele Identifier: CA3218800
Gene: PDZD2 HGNC NCBI

Linked Data

dbSNP Id: rs368664294

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.32000302del , CM000667.2:g.32000302del GRCh38
NC_000005.9:g.32000408del , CM000667.1:g.32000408del GRCh37
NC_000005.8:g.32036165del NCBI36
NG_033962.1:g.206379del
NG_033962.2:g.365893del

Transcript Alleles

HGVS Amino-acid change
ENST00000438447.2:c.1254+31del MANE Select ENSP00000402033.1:n.1254+31del
ENST00000438447.1:c.1254+31del ENSP00000402033.1:n.1254+31del
ENST00000502489.5:n.1010+31del
NM_178140.2:c.1254+31del NP_835260.2:n.1254+31del
XM_005248269.3:c.1254+31del XP_005248326.1:n.1254+31del
XM_005248270.3:c.1254+31del XP_005248327.1:n.1254+31del
XM_005248271.1:c.732+31del XP_005248328.1:n.732+31del
XM_005248272.3:c.732+31del XP_005248329.1:n.732+31del
XM_006714460.2:c.261+31del XP_006714523.1:n.261+31del
XM_011513992.1:c.1254+31del XP_011512294.1:n.1254+31del
XM_011513993.1:c.1254+31del XP_011512295.1:n.1254+31del
XM_011513994.1:c.1254+31del XP_011512296.1:n.1254+31del
XM_011513995.1:c.1254+31del XP_011512297.1:n.1254+31del
XM_011513996.1:c.979-10028del XP_011512298.1:n.979-10028del
XM_011513997.1:c.1254+31del XP_011512299.1:n.1254+31del
NM_178140.3:c.1254+31del NP_835260.2:n.1254+31del
XM_005248269.4:c.1254+31del XP_005248326.1:n.1254+31del
XM_005248272.4:c.732+31del XP_005248329.1:n.732+31del
XM_011513992.2:c.1254+31del XP_011512294.1:n.1254+31del
XM_011513993.2:c.1254+31del XP_011512295.1:n.1254+31del
XM_011513994.2:c.1254+31del XP_011512296.1:n.1254+31del
XM_011513995.2:c.1254+31del XP_011512297.1:n.1254+31del
XM_011513996.2:c.979-10028del XP_011512298.1:n.979-10028del
XM_017009245.1:c.457-10028del XP_016864734.1:n.457-10028del
XM_017009246.1:c.261+31del XP_016864735.1:n.261+31del
NM_178140.4:c.1254+31del MANE Select NP_835260.2:n.1254+31del