Canonical Allele Identifier: CA2059446606

Gene: PAH

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.102843712G= , CM000674.2:g.102843712G=	GRCh38
NC_000012.11:g.103237490G= , CM000674.1:g.103237490G=	GRCh37
NC_000012.10:g.101761620G=	NCBI36
NG_008690.1:g.78891C=
NG_008690.2:g.119699C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553106.6:c.1133C= MANE Select	ENSP00000448059.1:p.Thr378=
ENST00000307000.7:c.1118C=	ENSP00000303500.2:p.Thr373=
ENST00000549247.6:n.892C=
ENST00000551114.2:n.795C=
ENST00000553106.5:c.1133C=	ENSP00000448059.1:p.Thr378=
ENST00000635477.1:c.237C=
ENST00000635528.1:n.648C=
NM_000277.1:c.1133C=	NP_000268.1:p.Thr378=
XM_011538422.1:c.1076C=	XP_011536724.1:p.Thr359=
NM_000277.2:c.1133C=	NP_000268.1:p.Thr378=
NM_001354304.1:c.1133C=	NP_001341233.1:p.Thr378=
NM_000277.3:c.1133C= MANE Select	NP_000268.1:p.Thr378=
NM_001354304.2:c.1133C=	NP_001341233.1:p.Thr378=