Canonical Allele Identifier: CA10654658

Gene: PDCD10

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.167734846C>G , CM000665.2:g.167734846C>G	GRCh38
NC_000003.11:g.167452634C>G , CM000665.1:g.167452634C>G	GRCh37
NC_000003.10:g.168935328C>G	NCBI36
NG_008158.1:g.5018G>C
NG_008217.1:g.4203C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392750.7:c.-438G>C MANE Select	ENSP00000376506.2:n.-438G>C
ENST00000470131.5:c.-289G>C	ENSP00000417202.1:n.-289G>C
ENST00000471885.5:c.-190G>C	ENSP00000417876.1:n.-190G>C
ENST00000473645.6:c.-230G>C	ENSP00000418317.2:n.-230G>C
ENST00000481136.1:n.84G>C
ENST00000494502.6:c.-230G>C	ENSP00000420450.2:n.-230G>C
ENST00000497056.6:c.-157G>C	ENSP00000420553.2:n.-157G>C
NM_145859.1:c.-230G>C	NP_665858.1:n.-230G>C
XM_005247086.3:c.-289G>C	XP_005247143.1:n.-289G>C
XM_005247087.3:c.-294G>C	XP_005247144.1:n.-294G>C
XM_011512368.1:c.-362G>C	XP_011510670.1:n.-362G>C
XM_011512369.1:c.-367G>C	XP_011510671.1:n.-367G>C
XM_005247086.5:c.-289G>C	XP_005247143.1:n.-289G>C
XM_005247087.5:c.-294G>C	XP_005247144.1:n.-294G>C
XM_011512368.3:c.-362G>C	XP_011510670.1:n.-362G>C
XM_011512369.3:c.-367G>C	XP_011510671.1:n.-367G>C
XM_017005645.2:c.-474G>C	XP_016861134.1:n.-474G>C
XM_024453329.1:c.-547G>C	XP_024309097.1:n.-547G>C
XM_024453330.1:c.-679G>C	XP_024309098.1:n.-679G>C
XM_024453331.1:c.-606G>C	XP_024309099.1:n.-606G>C
NM_007217.4:c.-438G>C MANE Select	NP_009148.2:n.-438G>C
NM_145859.2:c.-230G>C	NP_665858.1:n.-230G>C
NM_145860.2:c.-157G>C	NP_665859.1:n.-157G>C