Canonical Allele Identifier: CA1418666339

Gene: PDCD10

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.167698899_167698901delinsCAA , CM000665.2:g.167698899_167698901delinsCAA	GRCh38
NC_000003.11:g.167416687_167416689delinsCAA , CM000665.1:g.167416687_167416689delinsCAA	GRCh37
NC_000003.10:g.168899381_168899383delinsCAA	NCBI36
NG_008158.1:g.40963_40965delinsTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392750.7:c.151-1775_151-1773delinsTTG MANE Select	ENSP00000376506.2:n.151-1775_151-1773delinsTTG
ENST00000392750.6:c.151-1775_151-1773delinsTTG	ENSP00000376506.2:n.151-1775_151-1773delinsTTG
ENST00000461494.5:c.151-1775_151-1773delinsTTG	ENSP00000420021.1:n.151-1775_151-1773delinsTTG
ENST00000462725.6:c.151-1775_151-1773delinsTTG	ENSP00000420424.2:n.151-1775_151-1773delinsTTG
ENST00000464360.5:c.151-1775_151-1773delinsTTG	ENSP00000418160.1:n.151-1775_151-1773delinsTTG
ENST00000470131.5:c.151-1775_151-1773delinsTTG	ENSP00000417202.1:n.151-1775_151-1773delinsTTG
ENST00000471885.5:c.151-1775_151-1773delinsTTG	ENSP00000417876.1:n.151-1775_151-1773delinsTTG
ENST00000473645.6:c.151-1775_151-1773delinsTTG	ENSP00000418317.2:n.151-1775_151-1773delinsTTG
ENST00000475915.6:c.151-1775_151-1773delinsTTG	ENSP00000417118.2:n.151-1775_151-1773delinsTTG
ENST00000479121.5:c.92-1775_92-1773delinsTTG
ENST00000483451.5:n.875-1775_875-1773delinsTTG
ENST00000487947.6:c.151-1775_151-1773delinsTTG	ENSP00000420266.2:n.151-1775_151-1773delinsTTG
ENST00000492139.5:c.151-1775_151-1773delinsTTG	ENSP00000420014.1:n.151-1775_151-1773delinsTTG
ENST00000492396.5:c.-39-1775_-39-1773delinsTTG	ENSP00000417309.1:n.-39-1775_-39-1773delinsTTG
ENST00000494502.6:c.151-923_151-921delinsTTG	ENSP00000420450.2:n.151-923_151-921delinsTTG
ENST00000497056.6:c.151-1775_151-1773delinsTTG	ENSP00000420553.2:n.151-1775_151-1773delinsTTG
NM_007217.3:c.151-1775_151-1773delinsTTG	NP_009148.2:n.151-1775_151-1773delinsTTG
NM_145859.1:c.151-1775_151-1773delinsTTG	NP_665858.1:n.151-1775_151-1773delinsTTG
NM_145860.1:c.151-1775_151-1773delinsTTG	NP_665859.1:n.151-1775_151-1773delinsTTG
XM_005247086.3:c.151-1775_151-1773delinsTTG	XP_005247143.1:n.151-1775_151-1773delinsTTG
XM_005247087.3:c.151-1775_151-1773delinsTTG	XP_005247144.1:n.151-1775_151-1773delinsTTG
XM_005247088.2:c.151-1775_151-1773delinsTTG	XP_005247145.1:n.151-1775_151-1773delinsTTG
XM_006713485.2:c.151-1775_151-1773delinsTTG	XP_006713548.1:n.151-1775_151-1773delinsTTG
XM_011512368.1:c.151-1775_151-1773delinsTTG	XP_011510670.1:n.151-1775_151-1773delinsTTG
XM_011512369.1:c.151-1775_151-1773delinsTTG	XP_011510671.1:n.151-1775_151-1773delinsTTG
XM_011512370.1:c.-167-923_-167-921delinsTTG	XP_011510672.1:n.-167-923_-167-921delinsTTG
XM_005247086.5:c.151-1775_151-1773delinsTTG	XP_005247143.1:n.151-1775_151-1773delinsTTG
XM_005247087.5:c.151-1775_151-1773delinsTTG	XP_005247144.1:n.151-1775_151-1773delinsTTG
XM_005247088.4:c.151-1775_151-1773delinsTTG	XP_005247145.1:n.151-1775_151-1773delinsTTG
XM_006713485.4:c.151-1775_151-1773delinsTTG	XP_006713548.1:n.151-1775_151-1773delinsTTG
XM_011512368.3:c.151-1775_151-1773delinsTTG	XP_011510670.1:n.151-1775_151-1773delinsTTG
XM_011512369.3:c.151-1775_151-1773delinsTTG	XP_011510671.1:n.151-1775_151-1773delinsTTG
XM_017005644.2:c.151-1775_151-1773delinsTTG	XP_016861133.1:n.151-1775_151-1773delinsTTG
XM_017005645.2:c.-167-923_-167-921delinsTTG	XP_016861134.1:n.-167-923_-167-921delinsTTG
XM_024453329.1:c.-167-923_-167-921delinsTTG	XP_024309097.1:n.-167-923_-167-921delinsTTG
XM_024453330.1:c.-167-923_-167-921delinsTTG	XP_024309098.1:n.-167-923_-167-921delinsTTG
XM_024453331.1:c.-167-923_-167-921delinsTTG	XP_024309099.1:n.-167-923_-167-921delinsTTG
NM_007217.4:c.151-1775_151-1773delinsTTG MANE Select	NP_009148.2:n.151-1775_151-1773delinsTTG
NM_145859.2:c.151-1775_151-1773delinsTTG	NP_665858.1:n.151-1775_151-1773delinsTTG
NM_145860.2:c.151-1775_151-1773delinsTTG	NP_665859.1:n.151-1775_151-1773delinsTTG