Canonical Allele Identifier: CA2059466388
Gene: PAH HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102894539T= , CM000674.2:g.102894539T= GRCh38
NC_000012.11:g.103288317T= , CM000674.1:g.103288317T= GRCh37
NC_000012.10:g.101812447T= NCBI36
NG_008690.1:g.28064A=
NG_008690.2:g.68872A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.352+196A= MANE Select ENSP00000448059.1:n.352+196A=
ENST00000307000.7:c.337+196A= ENSP00000303500.2:n.337+196A=
ENST00000548928.1:n.274+196A=
ENST00000549111.5:n.448+196A=
ENST00000550978.6:c.336+196A=
ENST00000551337.5:c.352+196A= ENSP00000447620.1:n.352+196A=
ENST00000551988.5:n.441+196A=
ENST00000553106.5:c.352+196A= ENSP00000448059.1:n.352+196A=
NM_000277.1:c.352+196A= NP_000268.1:n.352+196A=
XM_011538422.1:c.352+196A= XP_011536724.1:n.352+196A=
NM_000277.2:c.352+196A= NP_000268.1:n.352+196A=
NM_001354304.1:c.352+196A= NP_001341233.1:n.352+196A=
XM_017019370.2:c.352+196A= XP_016874859.1:n.352+196A=
NM_000277.3:c.352+196A= MANE Select NP_000268.1:n.352+196A=
NM_001354304.2:c.352+196A= NP_001341233.1:n.352+196A=
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