Canonical Allele Identifier: CA2059449533
Gene: PAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102855241G= , CM000674.2:g.102855241G= GRCh38
NC_000012.11:g.103249019G= , CM000674.1:g.103249019G= GRCh37
NC_000012.10:g.101773149G= NCBI36
NG_008690.1:g.67362C=
NG_008690.2:g.108170C=

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.601C= MANE Select ENSP00000448059.1:p.His201=
ENST00000307000.7:c.586C= ENSP00000303500.2:p.His196=
ENST00000549111.5:n.697C=
ENST00000553106.5:c.601C= ENSP00000448059.1:p.His201=
NM_000277.1:c.601C= NP_000268.1:p.His201=
XM_011538422.1:c.601C= XP_011536724.1:p.His201=
NM_000277.2:c.601C= NP_000268.1:p.His201=
NM_001354304.1:c.601C= NP_001341233.1:p.His201=
XM_017019370.2:c.601C= XP_016874859.1:p.His201=
NM_000277.3:c.601C= MANE Select NP_000268.1:p.His201=
NM_001354304.2:c.601C= NP_001341233.1:p.His201=