Canonical Allele Identifier: CA2059445981
Gene: PAH HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102852811T= , CM000674.2:g.102852811T= GRCh38
NC_000012.11:g.103246589T= , CM000674.1:g.103246589T= GRCh37
NC_000012.10:g.101770719T= NCBI36
NG_008690.1:g.69792A=
NG_008690.2:g.110600A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.842+4A= MANE Select ENSP00000448059.1:n.842+4A=
ENST00000307000.7:c.827+4A= ENSP00000303500.2:n.827+4A=
ENST00000549247.6:n.601+4A=
ENST00000553106.5:c.842+4A= ENSP00000448059.1:n.842+4A=
ENST00000635477.1:c.3+4A=
NM_000277.1:c.842+4A= NP_000268.1:n.842+4A=
XM_011538422.1:c.842+4A= XP_011536724.1:n.842+4A=
NM_000277.2:c.842+4A= NP_000268.1:n.842+4A=
NM_001354304.1:c.842+4A= NP_001341233.1:n.842+4A=
NM_000277.3:c.842+4A= MANE Select NP_000268.1:n.842+4A=
NM_001354304.2:c.842+4A= NP_001341233.1:n.842+4A=
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