Canonical Allele Identifier: CA5671908

Gene: PCGF6

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.103350892A>G , CM000672.2:g.103350892A>G	GRCh38
NC_000010.10:g.105110649A>G , CM000672.1:g.105110649A>G	GRCh37
NC_000010.9:g.105100639A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369847.4:c.175T>C MANE Select	ENSP00000358862.3:p.Ser59Pro
ENST00000647574.1:c.175T>C	ENSP00000497672.1:p.Ser59Pro
ENST00000337211.8:c.175T>C	ENSP00000338845.4:p.Ser59Pro
ENST00000369847.3:c.175T>C	ENSP00000358862.3:p.Ser59Pro
ENST00000490296.1:n.190T>C
NM_001011663.1:c.175T>C	NP_001011663.1:p.Ser59Pro
NM_032154.3:c.175T>C	NP_115530.2:p.Ser59Pro
XM_005270213.2:c.175T>C	XP_005270270.1:p.Ser59Pro
XM_011540261.1:c.175T>C	XP_011538563.1:p.Ser59Pro
XR_001747229.1:n.197T>C
XR_001747230.1:n.197T>C
NM_001011663.2:c.175T>C MANE Select	NP_001011663.1:p.Ser59Pro
NM_032154.4:c.175T>C	NP_115530.2:p.Ser59Pro