Canonical Allele Identifier: CA809838899

Gene: PDZD2

Linked Data

• dbSNP Id: rs1276645709
• MyVariant Identifiers: chr5:g.32000535_32000536insT (hg19) ; chr5:g.32000429_32000430insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.32000430dup , CM000667.2:g.32000430dup	GRCh38
NC_000005.9:g.32000536dup , CM000667.1:g.32000536dup	GRCh37
NC_000005.8:g.32036293dup	NCBI36
NG_033962.1:g.206507dup
NG_033962.2:g.366021dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000438447.2:c.1254+159dup MANE Select	ENSP00000402033.1:n.1254+159dup
ENST00000438447.1:c.1254+159dup	ENSP00000402033.1:n.1254+159dup
ENST00000502489.5:n.1010+159dup
NM_178140.2:c.1254+159dup	NP_835260.2:n.1254+159dup
XM_005248269.3:c.1254+159dup	XP_005248326.1:n.1254+159dup
XM_005248270.3:c.1254+159dup	XP_005248327.1:n.1254+159dup
XM_005248271.1:c.732+159dup	XP_005248328.1:n.732+159dup
XM_005248272.3:c.732+159dup	XP_005248329.1:n.732+159dup
XM_006714460.2:c.261+159dup	XP_006714523.1:n.261+159dup
XM_011513992.1:c.1254+159dup	XP_011512294.1:n.1254+159dup
XM_011513993.1:c.1254+159dup	XP_011512295.1:n.1254+159dup
XM_011513994.1:c.1254+159dup	XP_011512296.1:n.1254+159dup
XM_011513995.1:c.1254+159dup	XP_011512297.1:n.1254+159dup
XM_011513996.1:c.979-9900dup	XP_011512298.1:n.979-9900dup
XM_011513997.1:c.1254+159dup	XP_011512299.1:n.1254+159dup
NM_178140.3:c.1254+159dup	NP_835260.2:n.1254+159dup
XM_005248269.4:c.1254+159dup	XP_005248326.1:n.1254+159dup
XM_005248272.4:c.732+159dup	XP_005248329.1:n.732+159dup
XM_011513992.2:c.1254+159dup	XP_011512294.1:n.1254+159dup
XM_011513993.2:c.1254+159dup	XP_011512295.1:n.1254+159dup
XM_011513994.2:c.1254+159dup	XP_011512296.1:n.1254+159dup
XM_011513995.2:c.1254+159dup	XP_011512297.1:n.1254+159dup
XM_011513996.2:c.979-9900dup	XP_011512298.1:n.979-9900dup
XM_017009245.1:c.457-9900dup	XP_016864734.1:n.457-9900dup
XM_017009246.1:c.261+159dup	XP_016864735.1:n.261+159dup
NM_178140.4:c.1254+159dup MANE Select	NP_835260.2:n.1254+159dup