Canonical Allele Identifier: CA1537300117

Gene: PDZD2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.31999883T= , CM000667.2:g.31999883T=	GRCh38
NC_000005.9:g.31999989T= , CM000667.1:g.31999989T=	GRCh37
NC_000005.8:g.32035746T=	NCBI36
NG_033962.1:g.205960T=
NG_033962.2:g.365474T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000438447.2:c.1122-256T= MANE Select	ENSP00000402033.1:n.1122-256T=
ENST00000438447.1:c.1122-256T=	ENSP00000402033.1:n.1122-256T=
ENST00000502489.5:n.878-256T=
NM_178140.2:c.1122-256T=	NP_835260.2:n.1122-256T=
XM_005248269.3:c.1122-256T=	XP_005248326.1:n.1122-256T=
XM_005248270.3:c.1122-256T=	XP_005248327.1:n.1122-256T=
XM_005248271.1:c.600-256T=	XP_005248328.1:n.600-256T=
XM_005248272.3:c.600-256T=	XP_005248329.1:n.600-256T=
XM_006714460.2:c.129-256T=	XP_006714523.1:n.129-256T=
XM_011513992.1:c.1122-256T=	XP_011512294.1:n.1122-256T=
XM_011513993.1:c.1122-256T=	XP_011512295.1:n.1122-256T=
XM_011513994.1:c.1122-256T=	XP_011512296.1:n.1122-256T=
XM_011513995.1:c.1122-256T=	XP_011512297.1:n.1122-256T=
XM_011513996.1:c.979-10447T=	XP_011512298.1:n.979-10447T=
XM_011513997.1:c.1122-256T=	XP_011512299.1:n.1122-256T=
NM_178140.3:c.1122-256T=	NP_835260.2:n.1122-256T=
XM_005248269.4:c.1122-256T=	XP_005248326.1:n.1122-256T=
XM_005248272.4:c.600-256T=	XP_005248329.1:n.600-256T=
XM_011513992.2:c.1122-256T=	XP_011512294.1:n.1122-256T=
XM_011513993.2:c.1122-256T=	XP_011512295.1:n.1122-256T=
XM_011513994.2:c.1122-256T=	XP_011512296.1:n.1122-256T=
XM_011513995.2:c.1122-256T=	XP_011512297.1:n.1122-256T=
XM_011513996.2:c.979-10447T=	XP_011512298.1:n.979-10447T=
XM_017009245.1:c.457-10447T=	XP_016864734.1:n.457-10447T=
XM_017009246.1:c.129-256T=	XP_016864735.1:n.129-256T=
NM_178140.4:c.1122-256T= MANE Select	NP_835260.2:n.1122-256T=