Canonical Allele Identifier: CA2059476158

Gene: PAH

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.102917084G= , CM000674.2:g.102917084G=	GRCh38
NC_000012.11:g.103310862G= , CM000674.1:g.103310862G=	GRCh37
NC_000012.10:g.101834992G=	NCBI36
NG_008690.1:g.5519C=
NG_008690.2:g.46327C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553106.6:c.47C= MANE Select	ENSP00000448059.1:p.Ser16=
ENST00000307000.7:c.-101C=	ENSP00000303500.2:n.-101C=
ENST00000546844.1:c.47C=	ENSP00000446658.1:p.Ser16=
ENST00000547319.1:n.358C=
ENST00000549111.5:n.143C=
ENST00000550978.6:c.31C=
ENST00000551337.5:c.47C=	ENSP00000447620.1:p.Ser16=
ENST00000551988.5:n.136C=
ENST00000553106.5:c.47C=	ENSP00000448059.1:p.Ser16=
ENST00000635500.1:n.29-4186C=
NM_000277.1:c.47C=	NP_000268.1:p.Ser16=
XM_011538422.1:c.47C=	XP_011536724.1:p.Ser16=
NM_000277.2:c.47C=	NP_000268.1:p.Ser16=
NM_001354304.1:c.47C=	NP_001341233.1:p.Ser16=
XM_017019370.2:c.47C=	XP_016874859.1:p.Ser16=
NM_000277.3:c.47C= MANE Select	NP_000268.1:p.Ser16=
NM_001354304.2:c.47C=	NP_001341233.1:p.Ser16=