Canonical Allele Identifier: CA87829508

Gene: PDCD10

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.167734801C>T , CM000665.2:g.167734801C>T	GRCh38
NC_000003.11:g.167452589C>T , CM000665.1:g.167452589C>T	GRCh37
NC_000003.10:g.168935283C>T	NCBI36
NG_008158.1:g.5063G>A
NG_008217.1:g.4158C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_007217.4:c.-393G>A MANE Select	NP_009148.2:n.-393G>A
ENST00000392750.7:c.-393G>A MANE Select	ENSP00000376506.2:n.-393G>A
NM_007217.3:c.-393G>A	NP_009148.2:n.-393G>A
NM_145859.1:c.-190+5G>A	NP_665858.1:n.-190+5G>A
NM_145859.2:c.-190+5G>A	NP_665858.1:n.-190+5G>A
NM_145860.1:c.-117+5G>A	NP_665859.1:n.-117+5G>A
NM_145860.2:c.-117+5G>A	NP_665859.1:n.-117+5G>A
ENST00000392750.6:c.-393G>A	ENSP00000376506.2:n.-393G>A
ENST00000464360.5:c.-322+5G>A	ENSP00000418160.1:n.-322+5G>A
ENST00000470131.5:c.-249+5G>A	ENSP00000417202.1:n.-249+5G>A
ENST00000471885.5:c.-150+5G>A	ENSP00000417876.1:n.-150+5G>A
ENST00000473645.6:c.-190+5G>A	ENSP00000418317.2:n.-190+5G>A
ENST00000481136.1:n.124+5G>A
ENST00000483451.5:n.21G>A
ENST00000492139.5:c.-254+5G>A	ENSP00000420014.1:n.-254+5G>A
ENST00000494502.6:c.-190+5G>A	ENSP00000420450.2:n.-190+5G>A
ENST00000497056.6:c.-117+5G>A	ENSP00000420553.2:n.-117+5G>A
XM_005247086.3:c.-249+5G>A	XP_005247143.1:n.-249+5G>A
XM_005247086.5:c.-249+5G>A	XP_005247143.1:n.-249+5G>A
XM_005247087.3:c.-254+5G>A	XP_005247144.1:n.-254+5G>A
XM_005247087.5:c.-254+5G>A	XP_005247144.1:n.-254+5G>A
XM_011512368.1:c.-322+5G>A	XP_011510670.1:n.-322+5G>A
XM_011512368.3:c.-322+5G>A	XP_011510670.1:n.-322+5G>A
XM_011512369.1:c.-327+5G>A	XP_011510671.1:n.-327+5G>A
XM_011512369.3:c.-327+5G>A	XP_011510671.1:n.-327+5G>A
XM_017005645.2:c.-434+5G>A	XP_016861134.1:n.-434+5G>A
XM_024453329.1:c.-507+5G>A	XP_024309097.1:n.-507+5G>A
XM_024453330.1:c.-639+5G>A	XP_024309098.1:n.-639+5G>A
XM_024453331.1:c.-566+5G>A	XP_024309099.1:n.-566+5G>A