Canonical Allele Identifier: CA1537301120

Gene: PDZD2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.32000510_32000513delinsTTTG , CM000667.2:g.32000510_32000513delinsTTTG	GRCh38
NC_000005.9:g.32000616_32000619delinsTTTG , CM000667.1:g.32000616_32000619delinsTTTG	GRCh37
NC_000005.8:g.32036373_32036376delinsTTTG	NCBI36
NG_033962.1:g.206587_206590delinsTTTG
NG_033962.2:g.366101_366104delinsTTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000438447.2:c.1254+239_1254+242delinsTTTG MANE Select	ENSP00000402033.1:n.1254+239_1254+242delinsTTTG
ENST00000438447.1:c.1254+239_1254+242delinsTTTG	ENSP00000402033.1:n.1254+239_1254+242delinsTTTG
ENST00000502489.5:n.1010+239_1010+242delinsTTTG
NM_178140.2:c.1254+239_1254+242delinsTTTG	NP_835260.2:n.1254+239_1254+242delinsTTTG
XM_005248269.3:c.1254+239_1254+242delinsTTTG	XP_005248326.1:n.1254+239_1254+242delinsTTTG
XM_005248270.3:c.1254+239_1254+242delinsTTTG	XP_005248327.1:n.1254+239_1254+242delinsTTTG
XM_005248271.1:c.732+239_732+242delinsTTTG	XP_005248328.1:n.732+239_732+242delinsTTTG
XM_005248272.3:c.732+239_732+242delinsTTTG	XP_005248329.1:n.732+239_732+242delinsTTTG
XM_006714460.2:c.261+239_261+242delinsTTTG	XP_006714523.1:n.261+239_261+242delinsTTTG
XM_011513992.1:c.1254+239_1254+242delinsTTTG	XP_011512294.1:n.1254+239_1254+242delinsTTTG
XM_011513993.1:c.1254+239_1254+242delinsTTTG	XP_011512295.1:n.1254+239_1254+242delinsTTTG
XM_011513994.1:c.1254+239_1254+242delinsTTTG	XP_011512296.1:n.1254+239_1254+242delinsTTTG
XM_011513995.1:c.1254+239_1254+242delinsTTTG	XP_011512297.1:n.1254+239_1254+242delinsTTTG
XM_011513996.1:c.979-9820_979-9817delinsTTTG	XP_011512298.1:n.979-9820_979-9817delinsTTTG
XM_011513997.1:c.1254+239_1254+242delinsTTTG	XP_011512299.1:n.1254+239_1254+242delinsTTTG
NM_178140.3:c.1254+239_1254+242delinsTTTG	NP_835260.2:n.1254+239_1254+242delinsTTTG
XM_005248269.4:c.1254+239_1254+242delinsTTTG	XP_005248326.1:n.1254+239_1254+242delinsTTTG
XM_005248272.4:c.732+239_732+242delinsTTTG	XP_005248329.1:n.732+239_732+242delinsTTTG
XM_011513992.2:c.1254+239_1254+242delinsTTTG	XP_011512294.1:n.1254+239_1254+242delinsTTTG
XM_011513993.2:c.1254+239_1254+242delinsTTTG	XP_011512295.1:n.1254+239_1254+242delinsTTTG
XM_011513994.2:c.1254+239_1254+242delinsTTTG	XP_011512296.1:n.1254+239_1254+242delinsTTTG
XM_011513995.2:c.1254+239_1254+242delinsTTTG	XP_011512297.1:n.1254+239_1254+242delinsTTTG
XM_011513996.2:c.979-9820_979-9817delinsTTTG	XP_011512298.1:n.979-9820_979-9817delinsTTTG
XM_017009245.1:c.457-9820_457-9817delinsTTTG	XP_016864734.1:n.457-9820_457-9817delinsTTTG
XM_017009246.1:c.261+239_261+242delinsTTTG	XP_016864735.1:n.261+239_261+242delinsTTTG
NM_178140.4:c.1254+239_1254+242delinsTTTG MANE Select	NP_835260.2:n.1254+239_1254+242delinsTTTG