Canonical Allele Identifier: CA481332119
Gene: PAH HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.103260427A>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102866649A>T , CM000674.2:g.102866649A>T GRCh38
NC_000012.11:g.103260427A>T , CM000674.1:g.103260427A>T GRCh37
NC_000012.10:g.101784557A>T NCBI36
NG_008690.1:g.55954T>A
NG_008690.2:g.96762T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.456T>A MANE Select ENSP00000448059.1:p.Pro152=
ENST00000307000.7:c.441T>A ENSP00000303500.2:p.Pro147=
ENST00000549111.5:n.552T>A
ENST00000551988.5:n.530+10813T>A
ENST00000553106.5:c.456T>A ENSP00000448059.1:p.Pro152=
NM_000277.1:c.456T>A NP_000268.1:p.Pro152=
XM_011538422.1:c.456T>A XP_011536724.1:p.Pro152=
NM_000277.2:c.456T>A NP_000268.1:p.Pro152=
NM_001354304.1:c.456T>A NP_001341233.1:p.Pro152=
XM_017019370.2:c.456T>A XP_016874859.1:p.Pro152=
NM_000277.3:c.456T>A MANE Select NP_000268.1:p.Pro152=
NM_001354304.2:c.456T>A NP_001341233.1:p.Pro152=
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