Canonical Allele Identifier: CA2059441688

Gene: PAH

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.102840462G= , CM000674.2:g.102840462G=	GRCh38
NC_000012.11:g.103234240G= , CM000674.1:g.103234240G=	GRCh37
NC_000012.10:g.101758370G=	NCBI36
NG_008690.1:g.82141C=
NG_008690.2:g.122949C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553106.6:c.1253C= MANE Select	ENSP00000448059.1:p.Thr418=
ENST00000307000.7:c.1238C=	ENSP00000303500.2:p.Thr413=
ENST00000551114.2:n.915C=
ENST00000553106.5:c.1253C=	ENSP00000448059.1:p.Thr418=
ENST00000635477.1:c.357C=
ENST00000635528.1:n.768C=
NM_000277.1:c.1253C=	NP_000268.1:p.Thr418=
XM_011538422.1:c.1196C=	XP_011536724.1:p.Thr399=
NM_000277.2:c.1253C=	NP_000268.1:p.Thr418=
NM_001354304.1:c.1253C=	NP_001341233.1:p.Thr418=
NM_000277.3:c.1253C= MANE Select	NP_000268.1:p.Thr418=
NM_001354304.2:c.1253C=	NP_001341233.1:p.Thr418=