Canonical Allele Identifier: CA10615273

Gene: PDCD10

Linked Data

• ClinVar Variation Id: 344106
• ClinVar RCV Id: RCV000304562
• dbSNP Id: rs886058161
• gnomAD v4: 3-167684221-T-A
• MyVariant Identifiers: chr3:g.167402009T>A (hg19) ; chr3:g.167684221T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.167684221T>A , CM000665.2:g.167684221T>A	GRCh38
NC_000003.11:g.167402009T>A , CM000665.1:g.167402009T>A	GRCh37
NC_000003.10:g.168884703T>A	NCBI36
NG_008158.1:g.55643A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392750.7:c.*87A>T MANE Select	ENSP00000376506.2:n.*87A>T
ENST00000392750.6:c.*87A>T	ENSP00000376506.2:n.*87A>T
ENST00000473645.6:c.*87A>T	ENSP00000418317.2:n.*87A>T
ENST00000492396.5:c.*87A>T	ENSP00000417309.1:n.*87A>T
ENST00000497056.6:c.*87A>T	ENSP00000420553.2:n.*87A>T
NM_007217.3:c.*87A>T	NP_009148.2:n.*87A>T
NM_145859.1:c.*87A>T	NP_665858.1:n.*87A>T
NM_145860.1:c.*87A>T	NP_665859.1:n.*87A>T
XM_005247086.3:c.*87A>T	XP_005247143.1:n.*87A>T
XM_005247087.3:c.*87A>T	XP_005247144.1:n.*87A>T
XM_005247088.2:c.*87A>T	XP_005247145.1:n.*87A>T
XM_006713485.2:c.*87A>T	XP_006713548.1:n.*87A>T
XM_011512368.1:c.*87A>T	XP_011510670.1:n.*87A>T
XM_011512369.1:c.*87A>T	XP_011510671.1:n.*87A>T
XM_011512370.1:c.*87A>T	XP_011510672.1:n.*87A>T
XM_005247086.5:c.*87A>T	XP_005247143.1:n.*87A>T
XM_005247087.5:c.*87A>T	XP_005247144.1:n.*87A>T
XM_005247088.4:c.*87A>T	XP_005247145.1:n.*87A>T
XM_006713485.4:c.*87A>T	XP_006713548.1:n.*87A>T
XM_011512368.3:c.*87A>T	XP_011510670.1:n.*87A>T
XM_011512369.3:c.*87A>T	XP_011510671.1:n.*87A>T
XM_017005644.2:c.*87A>T	XP_016861133.1:n.*87A>T
XM_017005645.2:c.*87A>T	XP_016861134.1:n.*87A>T
XM_024453329.1:c.*87A>T	XP_024309097.1:n.*87A>T
XM_024453330.1:c.*87A>T	XP_024309098.1:n.*87A>T
XM_024453331.1:c.*87A>T	XP_024309099.1:n.*87A>T
NM_007217.4:c.*87A>T MANE Select	NP_009148.2:n.*87A>T
NM_145859.2:c.*87A>T	NP_665858.1:n.*87A>T
NM_145860.2:c.*87A>T	NP_665859.1:n.*87A>T