Canonical Allele Identifier: CA481332681
Gene: PAH HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.103271273G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102877495G>A , CM000674.2:g.102877495G>A GRCh38
NC_000012.11:g.103271273G>A , CM000674.1:g.103271273G>A GRCh37
NC_000012.10:g.101795403G>A NCBI36
NG_008690.1:g.45108C>T
NG_008690.2:g.85916C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.408C>T MANE Select ENSP00000448059.1:p.Leu136=
ENST00000307000.7:c.393C>T ENSP00000303500.2:p.Leu131=
ENST00000549111.5:n.504C>T
ENST00000550978.6:c.392C>T
ENST00000551337.5:c.408C>T ENSP00000447620.1:p.Leu136=
ENST00000551988.5:n.497C>T
ENST00000553106.5:c.408C>T ENSP00000448059.1:p.Leu136=
NM_000277.1:c.408C>T NP_000268.1:p.Leu136=
XM_011538422.1:c.408C>T XP_011536724.1:p.Leu136=
NM_000277.2:c.408C>T NP_000268.1:p.Leu136=
NM_001354304.1:c.408C>T NP_001341233.1:p.Leu136=
XM_017019370.2:c.408C>T XP_016874859.1:p.Leu136=
NM_000277.3:c.408C>T MANE Select NP_000268.1:p.Leu136=
NM_001354304.2:c.408C>T NP_001341233.1:p.Leu136=
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