Canonical Allele Identifier: CA2059449030
Gene: PAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102855140C= , CM000674.2:g.102855140C= GRCh38
NC_000012.11:g.103248918C= , CM000674.1:g.103248918C= GRCh37
NC_000012.10:g.101773048C= NCBI36
NG_008690.1:g.67463G=
NG_008690.2:g.108271G=

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.702G= MANE Select ENSP00000448059.1:p.Leu234=
ENST00000307000.7:c.687G= ENSP00000303500.2:p.Leu229=
ENST00000549111.5:n.798G=
ENST00000553106.5:c.702G= ENSP00000448059.1:p.Leu234=
NM_000277.1:c.702G= NP_000268.1:p.Leu234=
XM_011538422.1:c.702G= XP_011536724.1:p.Leu234=
NM_000277.2:c.702G= NP_000268.1:p.Leu234=
NM_001354304.1:c.702G= NP_001341233.1:p.Leu234=
XM_017019370.2:c.702G= XP_016874859.1:p.Leu234=
NM_000277.3:c.702G= MANE Select NP_000268.1:p.Leu234=
NM_001354304.2:c.702G= NP_001341233.1:p.Leu234=