Canonical Allele Identifier: CA2797241951
Gene: PAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102846603_102846604insTCGTTTCTAATTTTAGT , CM000674.2:g.102846603_102846604insTCGTTTCTAATTTTAGT GRCh38
NC_000012.11:g.103240381_103240382insTCGTTTCTAATTTTAGT , CM000674.1:g.103240381_103240382insTCGTTTCTAATTTTAGT GRCh37
NC_000012.10:g.101764511_101764512insTCGTTTCTAATTTTAGT NCBI36
NG_008690.1:g.75999_76000insACTAAAATTAGAAACGA
NG_008690.2:g.116807_116808insACTAAAATTAGAAACGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.969+291_969+292insACTAAAATTAGAAACGA MANE Select ENSP00000448059.1:n.969+291_969+292insACTAAAATTAGAAACGA
ENST00000307000.7:c.954+291_954+292insACTAAAATTAGAAACGA ENSP00000303500.2:n.954+291_954+292insACTAAAATTAGAAACGA
ENST00000549247.6:n.728+291_728+292insACTAAAATTAGAAACGA
ENST00000551114.2:n.631+291_631+292insACTAAAATTAGAAACGA
ENST00000553106.5:c.969+291_969+292insACTAAAATTAGAAACGA ENSP00000448059.1:n.969+291_969+292insACTAAAATTAGAAACGA
ENST00000635477.1:c.74-2173_74-2172insACTAAAATTAGAAACGA
ENST00000635528.1:n.484+291_484+292insACTAAAATTAGAAACGA
NM_000277.1:c.969+291_969+292insACTAAAATTAGAAACGA NP_000268.1:n.969+291_969+292insACTAAAATTAGAAACGA
XM_011538422.1:c.913-2173_913-2172insACTAAAATTAGAAACGA XP_011536724.1:n.913-2173_913-2172insACTAAAATTAGAAACGA
NM_000277.2:c.969+291_969+292insACTAAAATTAGAAACGA NP_000268.1:n.969+291_969+292insACTAAAATTAGAAACGA
NM_001354304.1:c.969+291_969+292insACTAAAATTAGAAACGA NP_001341233.1:n.969+291_969+292insACTAAAATTAGAAACGA
NM_000277.3:c.969+291_969+292insACTAAAATTAGAAACGA MANE Select NP_000268.1:n.969+291_969+292insACTAAAATTAGAAACGA
NM_001354304.2:c.969+291_969+292insACTAAAATTAGAAACGA NP_001341233.1:n.969+291_969+292insACTAAAATTAGAAACGA