Canonical Allele Identifier: CA2059462542
Gene: PAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102877629G= , CM000674.2:g.102877629G= GRCh38
NC_000012.11:g.103271407G= , CM000674.1:g.103271407G= GRCh37
NC_000012.10:g.101795537G= NCBI36
NG_008690.1:g.44974C=
NG_008690.2:g.85782C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.353-79C= MANE Select ENSP00000448059.1:n.353-79C=
ENST00000307000.7:c.338-79C= ENSP00000303500.2:n.338-79C=
ENST00000549111.5:n.449-79C=
ENST00000550978.6:c.337-79C=
ENST00000551337.5:c.353-79C= ENSP00000447620.1:n.353-79C=
ENST00000551988.5:n.442-79C=
ENST00000553106.5:c.353-79C= ENSP00000448059.1:n.353-79C=
NM_000277.1:c.353-79C= NP_000268.1:n.353-79C=
XM_011538422.1:c.353-79C= XP_011536724.1:n.353-79C=
NM_000277.2:c.353-79C= NP_000268.1:n.353-79C=
NM_001354304.1:c.353-79C= NP_001341233.1:n.353-79C=
XM_017019370.2:c.353-79C= XP_016874859.1:n.353-79C=
NM_000277.3:c.353-79C= MANE Select NP_000268.1:n.353-79C=
NM_001354304.2:c.353-79C= NP_001341233.1:n.353-79C=