Canonical Allele Identifier: CA2059446564
Gene: PAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102852910A= , CM000674.2:g.102852910A= GRCh38
NC_000012.11:g.103246688A= , CM000674.1:g.103246688A= GRCh37
NC_000012.10:g.101770818A= NCBI36
NG_008690.1:g.69693T=
NG_008690.2:g.110501T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.747T= MANE Select ENSP00000448059.1:p.Leu249=
ENST00000307000.7:c.732T= ENSP00000303500.2:p.Leu244=
ENST00000549247.6:n.506T=
ENST00000553106.5:c.747T= ENSP00000448059.1:p.Leu249=
NM_000277.1:c.747T= NP_000268.1:p.Leu249=
XM_011538422.1:c.747T= XP_011536724.1:p.Leu249=
NM_000277.2:c.747T= NP_000268.1:p.Leu249=
NM_001354304.1:c.747T= NP_001341233.1:p.Leu249=
NM_000277.3:c.747T= MANE Select NP_000268.1:p.Leu249=
NM_001354304.2:c.747T= NP_001341233.1:p.Leu249=