Canonical Allele Identifier: CA723026763
Gene: PHAF1 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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