Canonical Allele Identifier: CA115832563
Gene: PDZD2 HGNC NCBI

Linked Data

dbSNP Id: rs770515363

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.32000513_32000517del , CM000667.2:g.32000513_32000517del GRCh38
NC_000005.9:g.32000619_32000623del , CM000667.1:g.32000619_32000623del GRCh37
NC_000005.8:g.32036376_32036380del NCBI36
NG_033962.1:g.206590_206594del
NG_033962.2:g.366104_366108del

Transcript Alleles

HGVS Amino-acid Change
ENST00000438447.2:c.1254+242_1254+246del MANE Select ENSP00000402033.1:n.1254+242_1254+246del
ENST00000438447.1:c.1254+242_1254+246del ENSP00000402033.1:n.1254+242_1254+246del
ENST00000502489.5:n.1010+242_1010+246del
NM_178140.2:c.1254+242_1254+246del NP_835260.2:n.1254+242_1254+246del
XM_005248269.3:c.1254+242_1254+246del XP_005248326.1:n.1254+242_1254+246del
XM_005248270.3:c.1254+242_1254+246del XP_005248327.1:n.1254+242_1254+246del
XM_005248271.1:c.732+242_732+246del XP_005248328.1:n.732+242_732+246del
XM_005248272.3:c.732+242_732+246del XP_005248329.1:n.732+242_732+246del
XM_006714460.2:c.261+242_261+246del XP_006714523.1:n.261+242_261+246del
XM_011513992.1:c.1254+242_1254+246del XP_011512294.1:n.1254+242_1254+246del
XM_011513993.1:c.1254+242_1254+246del XP_011512295.1:n.1254+242_1254+246del
XM_011513994.1:c.1254+242_1254+246del XP_011512296.1:n.1254+242_1254+246del
XM_011513995.1:c.1254+242_1254+246del XP_011512297.1:n.1254+242_1254+246del
XM_011513996.1:c.979-9817_979-9813del XP_011512298.1:n.979-9817_979-9813del
XM_011513997.1:c.1254+242_1254+246del XP_011512299.1:n.1254+242_1254+246del
NM_178140.3:c.1254+242_1254+246del NP_835260.2:n.1254+242_1254+246del
XM_005248269.4:c.1254+242_1254+246del XP_005248326.1:n.1254+242_1254+246del
XM_005248272.4:c.732+242_732+246del XP_005248329.1:n.732+242_732+246del
XM_011513992.2:c.1254+242_1254+246del XP_011512294.1:n.1254+242_1254+246del
XM_011513993.2:c.1254+242_1254+246del XP_011512295.1:n.1254+242_1254+246del
XM_011513994.2:c.1254+242_1254+246del XP_011512296.1:n.1254+242_1254+246del
XM_011513995.2:c.1254+242_1254+246del XP_011512297.1:n.1254+242_1254+246del
XM_011513996.2:c.979-9817_979-9813del XP_011512298.1:n.979-9817_979-9813del
XM_017009245.1:c.457-9817_457-9813del XP_016864734.1:n.457-9817_457-9813del
XM_017009246.1:c.261+242_261+246del XP_016864735.1:n.261+242_261+246del
NM_178140.4:c.1254+242_1254+246del MANE Select NP_835260.2:n.1254+242_1254+246del