Canonical Allele Identifier: CA1537300642
Gene: PDZD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.32000235C= , CM000667.2:g.32000235C= GRCh38
NC_000005.9:g.32000341C= , CM000667.1:g.32000341C= GRCh37
NC_000005.8:g.32036098C= NCBI36
NG_033962.1:g.206312C=
NG_033962.2:g.365826C=

Transcript Alleles

HGVS Amino-acid change
ENST00000438447.2:c.1218C= MANE Select ENSP00000402033.1:p.Ser406=
ENST00000438447.1:c.1218C= ENSP00000402033.1:p.Ser406=
ENST00000502489.5:n.974C=
NM_178140.2:c.1218C= NP_835260.2:p.Ser406=
XM_005248269.3:c.1218C= XP_005248326.1:p.Ser406=
XM_005248270.3:c.1218C= XP_005248327.1:p.Ser406=
XM_005248271.1:c.696C= XP_005248328.1:p.Ser232=
XM_005248272.3:c.696C= XP_005248329.1:p.Ser232=
XM_006714460.2:c.225C= XP_006714523.1:p.Ser75=
XM_011513992.1:c.1218C= XP_011512294.1:p.Ser406=
XM_011513993.1:c.1218C= XP_011512295.1:p.Ser406=
XM_011513994.1:c.1218C= XP_011512296.1:p.Ser406=
XM_011513995.1:c.1218C= XP_011512297.1:p.Ser406=
XM_011513996.1:c.979-10095C= XP_011512298.1:n.979-10095C=
XM_011513997.1:c.1218C= XP_011512299.1:p.Ser406=
NM_178140.3:c.1218C= NP_835260.2:p.Ser406=
XM_005248269.4:c.1218C= XP_005248326.1:p.Ser406=
XM_005248272.4:c.696C= XP_005248329.1:p.Ser232=
XM_011513992.2:c.1218C= XP_011512294.1:p.Ser406=
XM_011513993.2:c.1218C= XP_011512295.1:p.Ser406=
XM_011513994.2:c.1218C= XP_011512296.1:p.Ser406=
XM_011513995.2:c.1218C= XP_011512297.1:p.Ser406=
XM_011513996.2:c.979-10095C= XP_011512298.1:n.979-10095C=
XM_017009245.1:c.457-10095C= XP_016864734.1:n.457-10095C=
XM_017009246.1:c.225C= XP_016864735.1:p.Ser75=
NM_178140.4:c.1218C= MANE Select NP_835260.2:p.Ser406=