Canonical Allele Identifier: CA2694506

Gene: PDCD10

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.167684373C>T , CM000665.2:g.167684373C>T	GRCh38
NC_000003.11:g.167402161C>T , CM000665.1:g.167402161C>T	GRCh37
NC_000003.10:g.168884855C>T	NCBI36
NG_008158.1:g.55491G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_007217.4:c.574G>A MANE Select	NP_009148.2:p.Val192Ile
ENST00000392750.7:c.574G>A MANE Select	ENSP00000376506.2:p.Val192Ile
NM_007217.3:c.574G>A	NP_009148.2:p.Val192Ile
NM_145859.1:c.574G>A	NP_665858.1:p.Val192Ile
NM_145859.2:c.574G>A	NP_665858.1:p.Val192Ile
NM_145860.1:c.574G>A	NP_665859.1:p.Val192Ile
NM_145860.2:c.574G>A	NP_665859.1:p.Val192Ile
ENST00000392750.6:c.574G>A	ENSP00000376506.2:p.Val192Ile
ENST00000461494.5:c.574G>A	ENSP00000420021.1:p.Val192Ile
ENST00000470131.5:c.574G>A	ENSP00000417202.1:p.Val192Ile
ENST00000473645.6:c.574G>A	ENSP00000418317.2:p.Val192Ile
ENST00000475915.6:c.574G>A	ENSP00000417118.2:p.Val192Ile
ENST00000492396.5:c.385G>A	ENSP00000417309.1:p.Val129Ile
ENST00000497056.6:c.574G>A	ENSP00000420553.2:p.Val192Ile
XM_005247086.3:c.574G>A	XP_005247143.1:p.Val192Ile
XM_005247086.5:c.574G>A	XP_005247143.1:p.Val192Ile
XM_005247087.3:c.574G>A	XP_005247144.1:p.Val192Ile
XM_005247087.5:c.574G>A	XP_005247144.1:p.Val192Ile
XM_005247088.2:c.574G>A	XP_005247145.1:p.Val192Ile
XM_005247088.4:c.574G>A	XP_005247145.1:p.Val192Ile
XM_006713485.2:c.574G>A	XP_006713548.1:p.Val192Ile
XM_006713485.4:c.574G>A	XP_006713548.1:p.Val192Ile
XM_011512368.1:c.574G>A	XP_011510670.1:p.Val192Ile
XM_011512368.3:c.574G>A	XP_011510670.1:p.Val192Ile
XM_011512369.1:c.574G>A	XP_011510671.1:p.Val192Ile
XM_011512369.3:c.574G>A	XP_011510671.1:p.Val192Ile
XM_011512370.1:c.385G>A	XP_011510672.1:p.Val129Ile
XM_017005644.2:c.574G>A	XP_016861133.1:p.Val192Ile
XM_017005645.2:c.385G>A	XP_016861134.1:p.Val129Ile
XM_024453329.1:c.385G>A	XP_024309097.1:p.Val129Ile
XM_024453330.1:c.385G>A	XP_024309098.1:p.Val129Ile
XM_024453331.1:c.385G>A	XP_024309099.1:p.Val129Ile