Canonical Allele Identifier: CA2059462477
Gene: PAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102877492G= , CM000674.2:g.102877492G= GRCh38
NC_000012.11:g.103271270G= , CM000674.1:g.103271270G= GRCh37
NC_000012.10:g.101795400G= NCBI36
NG_008690.1:g.45111C=
NG_008690.2:g.85919C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.411C= MANE Select ENSP00000448059.1:p.Ser137=
ENST00000307000.7:c.396C= ENSP00000303500.2:p.Ser132=
ENST00000549111.5:n.507C=
ENST00000550978.6:c.395C=
ENST00000551988.5:n.500C=
ENST00000553106.5:c.411C= ENSP00000448059.1:p.Ser137=
NM_000277.1:c.411C= NP_000268.1:p.Ser137=
XM_011538422.1:c.411C= XP_011536724.1:p.Ser137=
NM_000277.2:c.411C= NP_000268.1:p.Ser137=
NM_001354304.1:c.411C= NP_001341233.1:p.Ser137=
XM_017019370.2:c.411C= XP_016874859.1:p.Ser137=
NM_000277.3:c.411C= MANE Select NP_000268.1:p.Ser137=
NM_001354304.2:c.411C= NP_001341233.1:p.Ser137=