Canonical Allele Identifier: CA3197749618
Community Standard Title: NM_000277.3(PAH):c.912+658T=
Gene: PAH HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102851029A= , CM000674.2:g.102851029A= GRCh38
NC_000012.11:g.103244807A= , CM000674.1:g.103244807A= GRCh37
NC_000012.10:g.101768937A= NCBI36
NG_008690.1:g.71574T=
NG_008690.2:g.112382T=

Transcript Alleles

HGVS Amino-acid Change
NM_000277.3:c.912+658T= MANE Select NP_000268.1:n.912+658T=
ENST00000553106.6:c.912+658T= MANE Select ENSP00000448059.1:n.912+658T=
NM_000277.1:c.912+658T= NP_000268.1:n.912+658T=
NM_000277.2:c.912+658T= NP_000268.1:n.912+658T=
NM_001354304.1:c.912+658T= NP_001341233.1:n.912+658T=
NM_001354304.2:c.912+658T= NP_001341233.1:n.912+658T=
ENST00000307000.7:c.897+658T= ENSP00000303500.2:n.897+658T=
ENST00000549247.6:n.671+658T=
ENST00000551114.2:n.574+658T=
ENST00000553106.5:c.912+658T= ENSP00000448059.1:n.912+658T=
ENST00000635477.1:c.73+658T=
XM_011538422.1:c.912+658T= XP_011536724.1:n.912+658T=
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