Canonical Allele Identifier: CA2059446655
Gene: PAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102852924C= , CM000674.2:g.102852924C= GRCh38
NC_000012.11:g.103246702C= , CM000674.1:g.103246702C= GRCh37
NC_000012.10:g.101770832C= NCBI36
NG_008690.1:g.69679G=
NG_008690.2:g.110487G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.733G= MANE Select ENSP00000448059.1:p.Val245=
ENST00000307000.7:c.718G= ENSP00000303500.2:p.Val240=
ENST00000549247.6:n.492G=
ENST00000553106.5:c.733G= ENSP00000448059.1:p.Val245=
NM_000277.1:c.733G= NP_000268.1:p.Val245=
XM_011538422.1:c.733G= XP_011536724.1:p.Val245=
NM_000277.2:c.733G= NP_000268.1:p.Val245=
NM_001354304.1:c.733G= NP_001341233.1:p.Val245=
NM_000277.3:c.733G= MANE Select NP_000268.1:p.Val245=
NM_001354304.2:c.733G= NP_001341233.1:p.Val245=