Canonical Allele Identifier: CA2059441169
Gene: PAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102840260_102840261delinsAC , CM000674.2:g.102840260_102840261delinsAC GRCh38
NC_000012.11:g.103234038_103234039delinsAC , CM000674.1:g.103234038_103234039delinsAC GRCh37
NC_000012.10:g.101758168_101758169delinsAC NCBI36
NG_008690.1:g.82342_82343delinsGT
NG_008690.2:g.123150_123151delinsGT

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.1315+139_1315+140delinsGT MANE Select ENSP00000448059.1:n.1315+139_1315+140deli...
ENST00000307000.7:c.1300+139_1300+140delinsGT ENSP00000303500.2:n.1300+139_1300+140deli...
ENST00000551114.2:n.977+139_977+140delinsGT
ENST00000553106.5:c.1315+139_1315+140delinsGT ENSP00000448059.1:n.1315+139_1315+140deli...
ENST00000635477.1:c.419+139_419+140delinsGT
ENST00000635528.1:n.830+139_830+140delinsGT
NM_000277.1:c.1315+139_1315+140delinsGT NP_000268.1:n.1315+139_1315+140delinsGT
XM_011538422.1:c.1258+139_1258+140delinsGT XP_011536724.1:n.1258+139_1258+140delinsG...
NM_000277.2:c.1315+139_1315+140delinsGT NP_000268.1:n.1315+139_1315+140delinsGT
NM_001354304.1:c.1315+139_1315+140delinsGT NP_001341233.1:n.1315+139_1315+140delinsG...
NM_000277.3:c.1315+139_1315+140delinsGT MANE Select NP_000268.1:n.1315+139_1315+140delinsGT
NM_001354304.2:c.1315+139_1315+140delinsGT NP_001341233.1:n.1315+139_1315+140delinsG...