Canonical Allele Identifier: CA5671832

Gene: PCGF6

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.103348798T>C , CM000672.2:g.103348798T>C	GRCh38
NC_000010.10:g.105108555T>C , CM000672.1:g.105108555T>C	GRCh37
NC_000010.9:g.105098545T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001011663.2:c.475A>G MANE Select	NP_001011663.1:p.Ile159Val
ENST00000369847.4:c.475A>G MANE Select	ENSP00000358862.3:p.Ile159Val
NM_001011663.1:c.475A>G	NP_001011663.1:p.Ile159Val
NM_032154.3:c.475A>G	NP_115530.2:p.Ile159Val
NM_032154.4:c.475A>G	NP_115530.2:p.Ile159Val
ENST00000337211.8:c.475A>G	ENSP00000338845.4:p.Ile159Val
ENST00000369847.3:c.475A>G	ENSP00000358862.3:p.Ile159Val
ENST00000490296.1:n.490A>G
ENST00000492755.1:n.55A>G
ENST00000647574.1:c.475A>G	ENSP00000497672.1:p.Ile159Val
XM_005270213.2:c.475A>G	XP_005270270.1:p.Ile159Val
XM_011540261.1:c.475A>G	XP_011538563.1:p.Ile159Val
XR_001747229.1:n.497A>G
XR_001747230.1:n.497A>G