Canonical Allele Identifier: CA359340779

Gene: PDZD2

Linked Data

• MyVariant Identifiers: chr5:g.32000314C>G (hg19) ; chr5:g.32000208C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.32000208C>G , CM000667.2:g.32000208C>G	GRCh38
NC_000005.9:g.32000314C>G , CM000667.1:g.32000314C>G	GRCh37
NC_000005.8:g.32036071C>G	NCBI36
NG_033962.1:g.206285C>G
NG_033962.2:g.365799C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000438447.2:c.1191C>G MANE Select	ENSP00000402033.1:p.His397Gln
ENST00000438447.1:c.1191C>G	ENSP00000402033.1:p.His397Gln
ENST00000502489.5:n.947C>G
NM_178140.2:c.1191C>G	NP_835260.2:p.His397Gln
XM_005248269.3:c.1191C>G	XP_005248326.1:p.His397Gln
XM_005248270.3:c.1191C>G	XP_005248327.1:p.His397Gln
XM_005248271.1:c.669C>G	XP_005248328.1:p.His223Gln
XM_005248272.3:c.669C>G	XP_005248329.1:p.His223Gln
XM_006714460.2:c.198C>G	XP_006714523.1:p.His66Gln
XM_011513992.1:c.1191C>G	XP_011512294.1:p.His397Gln
XM_011513993.1:c.1191C>G	XP_011512295.1:p.His397Gln
XM_011513994.1:c.1191C>G	XP_011512296.1:p.His397Gln
XM_011513995.1:c.1191C>G	XP_011512297.1:p.His397Gln
XM_011513996.1:c.979-10122C>G	XP_011512298.1:n.979-10122C>G
XM_011513997.1:c.1191C>G	XP_011512299.1:p.His397Gln
NM_178140.3:c.1191C>G	NP_835260.2:p.His397Gln
XM_005248269.4:c.1191C>G	XP_005248326.1:p.His397Gln
XM_005248272.4:c.669C>G	XP_005248329.1:p.His223Gln
XM_011513992.2:c.1191C>G	XP_011512294.1:p.His397Gln
XM_011513993.2:c.1191C>G	XP_011512295.1:p.His397Gln
XM_011513994.2:c.1191C>G	XP_011512296.1:p.His397Gln
XM_011513995.2:c.1191C>G	XP_011512297.1:p.His397Gln
XM_011513996.2:c.979-10122C>G	XP_011512298.1:n.979-10122C>G
XM_017009245.1:c.457-10122C>G	XP_016864734.1:n.457-10122C>G
XM_017009246.1:c.198C>G	XP_016864735.1:p.His66Gln
NM_178140.4:c.1191C>G MANE Select	NP_835260.2:p.His397Gln