Canonical Allele Identifier: CA1537300134
Gene: PDZD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.31999888G= , CM000667.2:g.31999888G= GRCh38
NC_000005.9:g.31999994G= , CM000667.1:g.31999994G= GRCh37
NC_000005.8:g.32035751G= NCBI36
NG_033962.1:g.205965G=
NG_033962.2:g.365479G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000438447.2:c.1122-251G= MANE Select ENSP00000402033.1:n.1122-251G=
ENST00000438447.1:c.1122-251G= ENSP00000402033.1:n.1122-251G=
ENST00000502489.5:n.878-251G=
NM_178140.2:c.1122-251G= NP_835260.2:n.1122-251G=
XM_005248269.3:c.1122-251G= XP_005248326.1:n.1122-251G=
XM_005248270.3:c.1122-251G= XP_005248327.1:n.1122-251G=
XM_005248271.1:c.600-251G= XP_005248328.1:n.600-251G=
XM_005248272.3:c.600-251G= XP_005248329.1:n.600-251G=
XM_006714460.2:c.129-251G= XP_006714523.1:n.129-251G=
XM_011513992.1:c.1122-251G= XP_011512294.1:n.1122-251G=
XM_011513993.1:c.1122-251G= XP_011512295.1:n.1122-251G=
XM_011513994.1:c.1122-251G= XP_011512296.1:n.1122-251G=
XM_011513995.1:c.1122-251G= XP_011512297.1:n.1122-251G=
XM_011513996.1:c.979-10442G= XP_011512298.1:n.979-10442G=
XM_011513997.1:c.1122-251G= XP_011512299.1:n.1122-251G=
NM_178140.3:c.1122-251G= NP_835260.2:n.1122-251G=
XM_005248269.4:c.1122-251G= XP_005248326.1:n.1122-251G=
XM_005248272.4:c.600-251G= XP_005248329.1:n.600-251G=
XM_011513992.2:c.1122-251G= XP_011512294.1:n.1122-251G=
XM_011513993.2:c.1122-251G= XP_011512295.1:n.1122-251G=
XM_011513994.2:c.1122-251G= XP_011512296.1:n.1122-251G=
XM_011513995.2:c.1122-251G= XP_011512297.1:n.1122-251G=
XM_011513996.2:c.979-10442G= XP_011512298.1:n.979-10442G=
XM_017009245.1:c.457-10442G= XP_016864734.1:n.457-10442G=
XM_017009246.1:c.129-251G= XP_016864735.1:n.129-251G=
NM_178140.4:c.1122-251G= MANE Select NP_835260.2:n.1122-251G=