Canonical Allele Identifier: CA2059473203

Gene: PAH

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.102912777A= , CM000674.2:g.102912777A=	GRCh38
NC_000012.11:g.103306555A= , CM000674.1:g.103306555A=	GRCh37
NC_000012.10:g.101830685A=	NCBI36
NG_008690.1:g.9826T=
NG_008690.2:g.50634T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553106.6:c.168+14T= MANE Select	ENSP00000448059.1:n.168+14T=
ENST00000307000.7:c.153+14T=	ENSP00000303500.2:n.153+14T=
ENST00000546844.1:c.168+14T=	ENSP00000446658.1:n.168+14T=
ENST00000548677.2:n.255+14T=
ENST00000548928.1:n.90+14T=
ENST00000549111.5:n.264+14T=
ENST00000550978.6:c.152+14T=
ENST00000551337.5:c.168+14T=	ENSP00000447620.1:n.168+14T=
ENST00000551988.5:n.257+14T=
ENST00000553106.5:c.168+14T=	ENSP00000448059.1:n.168+14T=
ENST00000635500.1:n.136+14T=
NM_000277.1:c.168+14T=	NP_000268.1:n.168+14T=
XM_011538422.1:c.168+14T=	XP_011536724.1:n.168+14T=
NM_000277.2:c.168+14T=	NP_000268.1:n.168+14T=
NM_001354304.1:c.168+14T=	NP_001341233.1:n.168+14T=
XM_017019370.2:c.168+14T=	XP_016874859.1:n.168+14T=
NM_000277.3:c.168+14T= MANE Select	NP_000268.1:n.168+14T=
NM_001354304.2:c.168+14T=	NP_001341233.1:n.168+14T=