Canonical Allele Identifier: CA2059473459

Gene: PAH

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.102912848C= , CM000674.2:g.102912848C=	GRCh38
NC_000012.11:g.103306626C= , CM000674.1:g.103306626C=	GRCh37
NC_000012.10:g.101830756C=	NCBI36
NG_008690.1:g.9755G=
NG_008690.2:g.50563G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000553106.6:c.111G= MANE Select	ENSP00000448059.1:p.Leu37=
ENST00000307000.7:c.96G=	ENSP00000303500.2:p.Leu32=
ENST00000546844.1:c.111G=	ENSP00000446658.1:p.Leu37=
ENST00000548677.2:n.198G=
ENST00000548928.1:n.33G=
ENST00000549111.5:n.207G=
ENST00000550978.6:c.95G=
ENST00000551337.5:c.111G=	ENSP00000447620.1:p.Leu37=
ENST00000551988.5:n.200G=
ENST00000553106.5:c.111G=	ENSP00000448059.1:p.Leu37=
ENST00000635500.1:n.79G=
NM_000277.1:c.111G=	NP_000268.1:p.Leu37=
XM_011538422.1:c.111G=	XP_011536724.1:p.Leu37=
NM_000277.2:c.111G=	NP_000268.1:p.Leu37=
NM_001354304.1:c.111G=	NP_001341233.1:p.Leu37=
XM_017019370.2:c.111G=	XP_016874859.1:p.Leu37=
NM_000277.3:c.111G= MANE Select	NP_000268.1:p.Leu37=
NM_001354304.2:c.111G=	NP_001341233.1:p.Leu37=