Canonical Allele Identifier: CA2059441266
Gene: PAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102840338A= , CM000674.2:g.102840338A= GRCh38
NC_000012.11:g.103234116A= , CM000674.1:g.103234116A= GRCh37
NC_000012.10:g.101758246A= NCBI36
NG_008690.1:g.82265T=
NG_008690.2:g.123073T=

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.1315+62T= MANE Select ENSP00000448059.1:n.1315+62T=
ENST00000307000.7:c.1300+62T= ENSP00000303500.2:n.1300+62T=
ENST00000551114.2:n.977+62T=
ENST00000553106.5:c.1315+62T= ENSP00000448059.1:n.1315+62T=
ENST00000635477.1:c.419+62T=
ENST00000635528.1:n.830+62T=
NM_000277.1:c.1315+62T= NP_000268.1:n.1315+62T=
XM_011538422.1:c.1258+62T= XP_011536724.1:n.1258+62T=
NM_000277.2:c.1315+62T= NP_000268.1:n.1315+62T=
NM_001354304.1:c.1315+62T= NP_001341233.1:n.1315+62T=
NM_000277.3:c.1315+62T= MANE Select NP_000268.1:n.1315+62T=
NM_001354304.2:c.1315+62T= NP_001341233.1:n.1315+62T=