Canonical Allele Identifier: CA2059441879
Gene: PAH HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102840481C= , CM000674.2:g.102840481C= GRCh38
NC_000012.11:g.103234259C= , CM000674.1:g.103234259C= GRCh37
NC_000012.10:g.101758389C= NCBI36
NG_008690.1:g.82122G=
NG_008690.2:g.122930G=

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.1234G= MANE Select ENSP00000448059.1:p.Val412=
ENST00000307000.7:c.1219G= ENSP00000303500.2:p.Val407=
ENST00000551114.2:n.896G=
ENST00000553106.5:c.1234G= ENSP00000448059.1:p.Val412=
ENST00000635477.1:c.338G=
ENST00000635528.1:n.749G=
NM_000277.1:c.1234G= NP_000268.1:p.Val412=
XM_011538422.1:c.1177G= XP_011536724.1:p.Val393=
NM_000277.2:c.1234G= NP_000268.1:p.Val412=
NM_001354304.1:c.1234G= NP_001341233.1:p.Val412=
NM_000277.3:c.1234G= MANE Select NP_000268.1:p.Val412=
NM_001354304.2:c.1234G= NP_001341233.1:p.Val412=
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