Canonical Allele Identifier: CA2059456702
Gene: PAH HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102866024A= , CM000674.2:g.102866024A= GRCh38
NC_000012.11:g.103259802A= , CM000674.1:g.103259802A= GRCh37
NC_000012.10:g.101783932A= NCBI36
NG_008690.1:g.56579T=
NG_008690.2:g.97387T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.509+572T= MANE Select ENSP00000448059.1:n.509+572T=
ENST00000307000.7:c.494+572T= ENSP00000303500.2:n.494+572T=
ENST00000549111.5:n.605+572T=
ENST00000551988.5:n.531-10692T=
ENST00000553106.5:c.509+572T= ENSP00000448059.1:n.509+572T=
NM_000277.1:c.509+572T= NP_000268.1:n.509+572T=
XM_011538422.1:c.509+572T= XP_011536724.1:n.509+572T=
NM_000277.2:c.509+572T= NP_000268.1:n.509+572T=
NM_001354304.1:c.509+572T= NP_001341233.1:n.509+572T=
XM_017019370.2:c.509+572T= XP_016874859.1:n.509+572T=
NM_000277.3:c.509+572T= MANE Select NP_000268.1:n.509+572T=
NM_001354304.2:c.509+572T= NP_001341233.1:n.509+572T=
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