Canonical Allele Identifier: CA2059449370
Gene: PAH HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102855210G= , CM000674.2:g.102855210G= GRCh38
NC_000012.11:g.103248988G= , CM000674.1:g.103248988G= GRCh37
NC_000012.10:g.101773118G= NCBI36
NG_008690.1:g.67393C=
NG_008690.2:g.108201C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.632C= MANE Select ENSP00000448059.1:p.Pro211=
ENST00000307000.7:c.617C= ENSP00000303500.2:p.Pro206=
ENST00000549111.5:n.728C=
ENST00000553106.5:c.632C= ENSP00000448059.1:p.Pro211=
NM_000277.1:c.632C= NP_000268.1:p.Pro211=
XM_011538422.1:c.632C= XP_011536724.1:p.Pro211=
NM_000277.2:c.632C= NP_000268.1:p.Pro211=
NM_001354304.1:c.632C= NP_001341233.1:p.Pro211=
XM_017019370.2:c.632C= XP_016874859.1:p.Pro211=
NM_000277.3:c.632C= MANE Select NP_000268.1:p.Pro211=
NM_001354304.2:c.632C= NP_001341233.1:p.Pro211=
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