Canonical Allele Identifier: CA2059467064
Gene: PAH HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102894888A= , CM000674.2:g.102894888A= GRCh38
NC_000012.11:g.103288666A= , CM000674.1:g.103288666A= GRCh37
NC_000012.10:g.101812796A= NCBI36
NG_008690.1:g.27715T=
NG_008690.2:g.68523T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.199T= MANE Select ENSP00000448059.1:p.Ser67=
ENST00000307000.7:c.184T= ENSP00000303500.2:p.Ser62=
ENST00000546844.1:c.199T= ENSP00000446658.1:p.Ser67=
ENST00000548677.2:n.286T=
ENST00000548928.1:n.121T=
ENST00000549111.5:n.295T=
ENST00000550978.6:c.183T=
ENST00000551337.5:c.199T= ENSP00000447620.1:p.Ser67=
ENST00000551988.5:n.288T=
ENST00000553106.5:c.199T= ENSP00000448059.1:p.Ser67=
ENST00000635500.1:n.167T=
NM_000277.1:c.199T= NP_000268.1:p.Ser67=
XM_011538422.1:c.199T= XP_011536724.1:p.Ser67=
NM_000277.2:c.199T= NP_000268.1:p.Ser67=
NM_001354304.1:c.199T= NP_001341233.1:p.Ser67=
XM_017019370.2:c.199T= XP_016874859.1:p.Ser67=
NM_000277.3:c.199T= MANE Select NP_000268.1:p.Ser67=
NM_001354304.2:c.199T= NP_001341233.1:p.Ser67=
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