Canonical Allele Identifier: CA2059448791

Gene: PAH

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.102854997T= , CM000674.2:g.102854997T=	GRCh38
NC_000012.11:g.103248775T= , CM000674.1:g.103248775T=	GRCh37
NC_000012.10:g.101772905T=	NCBI36
NG_008690.1:g.67606A=
NG_008690.2:g.108414A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553106.6:c.706+139A= MANE Select	ENSP00000448059.1:n.706+139A=
ENST00000307000.7:c.691+139A=	ENSP00000303500.2:n.691+139A=
ENST00000549111.5:n.941A=
ENST00000553106.5:c.706+139A=	ENSP00000448059.1:n.706+139A=
NM_000277.1:c.706+139A=	NP_000268.1:n.706+139A=
XM_011538422.1:c.706+139A=	XP_011536724.1:n.706+139A=
NM_000277.2:c.706+139A=	NP_000268.1:n.706+139A=
NM_001354304.1:c.706+139A=	NP_001341233.1:n.706+139A=
XM_017019370.2:c.706+139A=	XP_016874859.1:n.706+139A=
NM_000277.3:c.706+139A= MANE Select	NP_000268.1:n.706+139A=
NM_001354304.2:c.706+139A=	NP_001341233.1:n.706+139A=