Canonical Allele Identifier: CA2059462461
Gene: PAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102877468G= , CM000674.2:g.102877468G= GRCh38
NC_000012.11:g.103271246G= , CM000674.1:g.103271246G= GRCh37
NC_000012.10:g.101795376G= NCBI36
NG_008690.1:g.45135C=
NG_008690.2:g.85943C=

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.435C= MANE Select ENSP00000448059.1:p.Asp145=
ENST00000307000.7:c.420C= ENSP00000303500.2:p.Asp140=
ENST00000549111.5:n.531C=
ENST00000550978.6:c.419C=
ENST00000551988.5:n.524C=
ENST00000553106.5:c.435C= ENSP00000448059.1:p.Asp145=
NM_000277.1:c.435C= NP_000268.1:p.Asp145=
XM_011538422.1:c.435C= XP_011536724.1:p.Asp145=
NM_000277.2:c.435C= NP_000268.1:p.Asp145=
NM_001354304.1:c.435C= NP_001341233.1:p.Asp145=
XM_017019370.2:c.435C= XP_016874859.1:p.Asp145=
NM_000277.3:c.435C= MANE Select NP_000268.1:p.Asp145=
NM_001354304.2:c.435C= NP_001341233.1:p.Asp145=