Canonical Allele Identifier: CA2059449026
Gene: PAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102855139G= , CM000674.2:g.102855139G= GRCh38
NC_000012.11:g.103248917G= , CM000674.1:g.103248917G= GRCh37
NC_000012.10:g.101773047G= NCBI36
NG_008690.1:g.67464C=
NG_008690.2:g.108272C=

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.703C= MANE Select ENSP00000448059.1:p.Gln235=
ENST00000307000.7:c.688C= ENSP00000303500.2:p.Gln230=
ENST00000549111.5:n.799C=
ENST00000553106.5:c.703C= ENSP00000448059.1:p.Gln235=
NM_000277.1:c.703C= NP_000268.1:p.Gln235=
XM_011538422.1:c.703C= XP_011536724.1:p.Gln235=
NM_000277.2:c.703C= NP_000268.1:p.Gln235=
NM_001354304.1:c.703C= NP_001341233.1:p.Gln235=
XM_017019370.2:c.703C= XP_016874859.1:p.Gln235=
NM_000277.3:c.703C= MANE Select NP_000268.1:p.Gln235=
NM_001354304.2:c.703C= NP_001341233.1:p.Gln235=