Canonical Allele Identifier: CA2059446631

Gene: PAH

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.102843716A= , CM000674.2:g.102843716A=	GRCh38
NC_000012.11:g.103237494A= , CM000674.1:g.103237494A=	GRCh37
NC_000012.10:g.101761624A=	NCBI36
NG_008690.1:g.78887T=
NG_008690.2:g.119695T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553106.6:c.1129T= MANE Select	ENSP00000448059.1:p.Tyr377=
ENST00000307000.7:c.1114T=	ENSP00000303500.2:p.Tyr372=
ENST00000549247.6:n.888T=
ENST00000551114.2:n.791T=
ENST00000553106.5:c.1129T=	ENSP00000448059.1:p.Tyr377=
ENST00000635477.1:c.233T=
ENST00000635528.1:n.644T=
NM_000277.1:c.1129T=	NP_000268.1:p.Tyr377=
XM_011538422.1:c.1072T=	XP_011536724.1:p.Tyr358=
NM_000277.2:c.1129T=	NP_000268.1:p.Tyr377=
NM_001354304.1:c.1129T=	NP_001341233.1:p.Tyr377=
NM_000277.3:c.1129T= MANE Select	NP_000268.1:p.Tyr377=
NM_001354304.2:c.1129T=	NP_001341233.1:p.Tyr377=