Canonical Allele Identifier: CA15866912

Gene: PHAF1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67148096A>G , CM000678.2:g.67148096A>G	GRCh38
NC_000016.9:g.67181999A>G , CM000678.1:g.67181999A>G	GRCh37
NC_000016.8:g.65739500A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219139.8:c.*965A>G MANE Select	ENSP00000219139.3:n.*965A>G
ENST00000219139.7:c.*965A>G	ENSP00000219139.3:n.*965A>G
NM_025187.3:c.*965A>G	NP_079463.2:n.*965A>G
XM_005256177.2:c.*965A>G	XP_005256234.1:n.*965A>G
XM_005256178.3:c.*965A>G	XP_005256235.1:n.*965A>G
XM_006721284.2:c.*965A>G	XP_006721347.1:n.*965A>G
XM_011523350.1:c.*965A>G	XP_011521652.1:n.*965A>G
NM_001320540.1:c.*965A>G	NP_001307469.1:n.*965A>G
NM_001320541.1:c.*965A>G	NP_001307470.1:n.*965A>G
NM_001320542.1:c.*965A>G	NP_001307471.1:n.*965A>G
NM_001320543.1:c.*965A>G	NP_001307472.1:n.*965A>G
NM_025187.4:c.*965A>G	NP_079463.2:n.*965A>G
XM_006721284.3:c.*965A>G	XP_006721347.1:n.*965A>G
XM_011523350.3:c.*965A>G	XP_011521652.1:n.*965A>G
XM_017023729.1:c.*965A>G	XP_016879218.1:n.*965A>G
NM_001320540.2:c.*965A>G	NP_001307469.1:n.*965A>G
NM_001320541.2:c.*965A>G	NP_001307470.1:n.*965A>G
NM_001320542.2:c.*965A>G	NP_001307471.1:n.*965A>G
NM_001320543.2:c.*965A>G	NP_001307472.1:n.*965A>G
NM_025187.5:c.*965A>G MANE Select	NP_079463.2:n.*965A>G