Canonical Allele Identifier: CA443642825

Gene: PDZD2

Linked Data

• MyVariant Identifiers: chr5:g.32000356G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.32000250G>C , CM000667.2:g.32000250G>C	GRCh38
NC_000005.9:g.32000356G>C , CM000667.1:g.32000356G>C	GRCh37
NC_000005.8:g.32036113G>C	NCBI36
NG_033962.1:g.206327G>C
NG_033962.2:g.365841G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000438447.2:c.1233G>C MANE Select	ENSP00000402033.1:p.Val411=
ENST00000438447.1:c.1233G>C	ENSP00000402033.1:p.Val411=
ENST00000502489.5:n.989G>C
NM_178140.2:c.1233G>C	NP_835260.2:p.Val411=
XM_005248269.3:c.1233G>C	XP_005248326.1:p.Val411=
XM_005248270.3:c.1233G>C	XP_005248327.1:p.Val411=
XM_005248271.1:c.711G>C	XP_005248328.1:p.Val237=
XM_005248272.3:c.711G>C	XP_005248329.1:p.Val237=
XM_006714460.2:c.240G>C	XP_006714523.1:p.Val80=
XM_011513992.1:c.1233G>C	XP_011512294.1:p.Val411=
XM_011513993.1:c.1233G>C	XP_011512295.1:p.Val411=
XM_011513994.1:c.1233G>C	XP_011512296.1:p.Val411=
XM_011513995.1:c.1233G>C	XP_011512297.1:p.Val411=
XM_011513996.1:c.979-10080G>C	XP_011512298.1:n.979-10080G>C
XM_011513997.1:c.1233G>C	XP_011512299.1:p.Val411=
NM_178140.3:c.1233G>C	NP_835260.2:p.Val411=
XM_005248269.4:c.1233G>C	XP_005248326.1:p.Val411=
XM_005248272.4:c.711G>C	XP_005248329.1:p.Val237=
XM_011513992.2:c.1233G>C	XP_011512294.1:p.Val411=
XM_011513993.2:c.1233G>C	XP_011512295.1:p.Val411=
XM_011513994.2:c.1233G>C	XP_011512296.1:p.Val411=
XM_011513995.2:c.1233G>C	XP_011512297.1:p.Val411=
XM_011513996.2:c.979-10080G>C	XP_011512298.1:n.979-10080G>C
XM_017009245.1:c.457-10080G>C	XP_016864734.1:n.457-10080G>C
XM_017009246.1:c.240G>C	XP_016864735.1:p.Val80=
NM_178140.4:c.1233G>C MANE Select	NP_835260.2:p.Val411=