Canonical Allele Identifier: CA115832546

Gene: PDZD2

Linked Data

• dbSNP Id: rs140415640
• gnomAD v2: 5-32000585-GTTTGTTTTTGTT-G
• gnomAD v3: 5-32000479-GTTTGTTTTTGTT-G
• gnomAD v4: 5-32000479-GTTTGTTTTTGTT-G
• COSMIC: COSN18729362 ; COSN20069563
• MyVariant Identifiers: chr5:g.32000598_32000609del (hg19) ; chr5:g.32000586_32000597del (hg19) ; chr5:g.32000492_32000503del (hg38) ; chr5:g.32000480_32000491del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.32000513_32000524del , CM000667.2:g.32000513_32000524del	GRCh38
NC_000005.9:g.32000619_32000630del , CM000667.1:g.32000619_32000630del	GRCh37
NC_000005.8:g.32036376_32036387del	NCBI36
NG_033962.1:g.206590_206601del
NG_033962.2:g.366104_366115del

Transcript Alleles

HGVS	Amino-acid change
ENST00000438447.2:c.1254+242_1254+253del MANE Select	ENSP00000402033.1:n.1254+242_1254+253del
ENST00000438447.1:c.1254+242_1254+253del	ENSP00000402033.1:n.1254+242_1254+253del
ENST00000502489.5:n.1010+242_1010+253del
NM_178140.2:c.1254+242_1254+253del	NP_835260.2:n.1254+242_1254+253del
XM_005248269.3:c.1254+242_1254+253del	XP_005248326.1:n.1254+242_1254+253del
XM_005248270.3:c.1254+242_1254+253del	XP_005248327.1:n.1254+242_1254+253del
XM_005248271.1:c.732+242_732+253del	XP_005248328.1:n.732+242_732+253del
XM_005248272.3:c.732+242_732+253del	XP_005248329.1:n.732+242_732+253del
XM_006714460.2:c.261+242_261+253del	XP_006714523.1:n.261+242_261+253del
XM_011513992.1:c.1254+242_1254+253del	XP_011512294.1:n.1254+242_1254+253del
XM_011513993.1:c.1254+242_1254+253del	XP_011512295.1:n.1254+242_1254+253del
XM_011513994.1:c.1254+242_1254+253del	XP_011512296.1:n.1254+242_1254+253del
XM_011513995.1:c.1254+242_1254+253del	XP_011512297.1:n.1254+242_1254+253del
XM_011513996.1:c.979-9817_979-9806del	XP_011512298.1:n.979-9817_979-9806del
XM_011513997.1:c.1254+242_1254+253del	XP_011512299.1:n.1254+242_1254+253del
NM_178140.3:c.1254+242_1254+253del	NP_835260.2:n.1254+242_1254+253del
XM_005248269.4:c.1254+242_1254+253del	XP_005248326.1:n.1254+242_1254+253del
XM_005248272.4:c.732+242_732+253del	XP_005248329.1:n.732+242_732+253del
XM_011513992.2:c.1254+242_1254+253del	XP_011512294.1:n.1254+242_1254+253del
XM_011513993.2:c.1254+242_1254+253del	XP_011512295.1:n.1254+242_1254+253del
XM_011513994.2:c.1254+242_1254+253del	XP_011512296.1:n.1254+242_1254+253del
XM_011513995.2:c.1254+242_1254+253del	XP_011512297.1:n.1254+242_1254+253del
XM_011513996.2:c.979-9817_979-9806del	XP_011512298.1:n.979-9817_979-9806del
XM_017009245.1:c.457-9817_457-9806del	XP_016864734.1:n.457-9817_457-9806del
XM_017009246.1:c.261+242_261+253del	XP_016864735.1:n.261+242_261+253del
NM_178140.4:c.1254+242_1254+253del MANE Select	NP_835260.2:n.1254+242_1254+253del