Canonical Allele Identifier: CA481375671
Gene: PAH HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.103237524G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102843746G>A , CM000674.2:g.102843746G>A GRCh38
NC_000012.11:g.103237524G>A , CM000674.1:g.103237524G>A GRCh37
NC_000012.10:g.101761654G>A NCBI36
NG_008690.1:g.78857C>T
NG_008690.2:g.119665C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.1099C>T MANE Select ENSP00000448059.1:p.Leu367=
ENST00000307000.7:c.1084C>T ENSP00000303500.2:p.Leu362=
ENST00000549247.6:n.858C>T
ENST00000551114.2:n.761C>T
ENST00000553106.5:c.1099C>T ENSP00000448059.1:p.Leu367=
ENST00000635477.1:c.203C>T
ENST00000635528.1:n.614C>T
NM_000277.1:c.1099C>T NP_000268.1:p.Leu367=
XM_011538422.1:c.1042C>T XP_011536724.1:p.Leu348=
NM_000277.2:c.1099C>T NP_000268.1:p.Leu367=
NM_001354304.1:c.1099C>T NP_001341233.1:p.Leu367=
NM_000277.3:c.1099C>T MANE Select NP_000268.1:p.Leu367=
NM_001354304.2:c.1099C>T NP_001341233.1:p.Leu367=
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