Canonical Allele Identifier: CA11674761
Gene: PCGF3 HGNC NCBI
gnomAD v2:
gnomAD v3:
gnomAD v4:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.741362G>A , CM000666.2:g.741362G>A GRCh38
NC_000004.11:g.735150G>A , CM000666.1:g.735150G>A GRCh37
NC_000004.10:g.725150G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000362003.10:c.263-2112G>A MANE Select ENSP00000354724.5:n.263-2112G>A
ENST00000362003.9:c.263-2112G>A ENSP00000354724.5:n.263-2112G>A
ENST00000430644.5:c.*965-2112G>A ENSP00000402946.1:n.*965-2112G>A
ENST00000433814.5:c.263-2112G>A ENSP00000398493.1:n.263-2112G>A
ENST00000440452.5:c.*965-2112G>A ENSP00000405840.1:n.*965-2112G>A
ENST00000470161.6:c.263-2112G>A ENSP00000420489.2:n.263-2112G>A
ENST00000505655.2:c.263-2112G>A ENSP00000423393.2:n.263-2112G>A
NM_006315.4:c.263-2112G>A NP_006306.2:n.263-2112G>A
XM_005272250.1:c.263-2112G>A XP_005272307.1:n.263-2112G>A
XM_005272253.1:c.161-2112G>A XP_005272310.1:n.161-2112G>A
XM_005272254.1:c.161-2112G>A XP_005272311.1:n.161-2112G>A
XM_006713852.1:c.161-2112G>A XP_006713915.1:n.161-2112G>A
XM_011513381.1:c.263-2112G>A XP_011511683.1:n.263-2112G>A
XM_011513382.1:c.263-2112G>A XP_011511684.1:n.263-2112G>A
XM_011513383.1:c.263-2112G>A XP_011511685.1:n.263-2112G>A
XM_011513384.1:c.263-2112G>A XP_011511686.1:n.263-2112G>A
XM_011513385.1:c.263-2112G>A XP_011511687.1:n.263-2112G>A
NM_001317836.1:c.263-2112G>A NP_001304765.1:n.263-2112G>A
NM_006315.5:c.263-2112G>A NP_006306.2:n.263-2112G>A
XR_001741543.1:n.1174G>A
NM_001317836.2:c.263-2112G>A NP_001304765.1:n.263-2112G>A
NM_006315.6:c.263-2112G>A NP_006306.2:n.263-2112G>A
NM_001317836.3:c.263-2112G>A NP_001304765.1:n.263-2112G>A
NM_001395245.1:c.263-2112G>A NP_001382174.1:n.263-2112G>A
NM_001395246.1:c.263-2112G>A NP_001382175.1:n.263-2112G>A
NM_001395247.1:c.263-2112G>A NP_001382176.1:n.263-2112G>A
NM_001395248.1:c.263-2112G>A NP_001382177.1:n.263-2112G>A
NM_001395249.1:c.263-2112G>A NP_001382178.1:n.263-2112G>A
NM_001395250.1:c.161-2112G>A NP_001382179.1:n.161-2112G>A
NM_001395251.1:c.161-2112G>A NP_001382180.1:n.161-2112G>A
NM_006315.7:c.263-2112G>A MANE Select NP_006306.2:n.263-2112G>A