Canonical Allele Identifier: CA2059446592
Gene: PAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102852915G= , CM000674.2:g.102852915G= GRCh38
NC_000012.11:g.103246693G= , CM000674.1:g.103246693G= GRCh37
NC_000012.10:g.101770823G= NCBI36
NG_008690.1:g.69688C=
NG_008690.2:g.110496C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.742C= MANE Select ENSP00000448059.1:p.Leu248=
ENST00000307000.7:c.727C= ENSP00000303500.2:p.Leu243=
ENST00000549247.6:n.501C=
ENST00000553106.5:c.742C= ENSP00000448059.1:p.Leu248=
NM_000277.1:c.742C= NP_000268.1:p.Leu248=
XM_011538422.1:c.742C= XP_011536724.1:p.Leu248=
NM_000277.2:c.742C= NP_000268.1:p.Leu248=
NM_001354304.1:c.742C= NP_001341233.1:p.Leu248=
NM_000277.3:c.742C= MANE Select NP_000268.1:p.Leu248=
NM_001354304.2:c.742C= NP_001341233.1:p.Leu248=