Canonical Allele Identifier: CA2838225755

Gene: PAH

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.102843864T>A , CM000674.2:g.102843864T>A	GRCh38
NC_000012.11:g.103237642T>A , CM000674.1:g.103237642T>A	GRCh37
NC_000012.10:g.101761772T>A	NCBI36
NG_008690.1:g.78739A>T
NG_008690.2:g.119547A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553106.6:c.1066-85A>T MANE Select	ENSP00000448059.1:n.1066-85A>T
ENST00000307000.7:c.1051-85A>T	ENSP00000303500.2:n.1051-85A>T
ENST00000549247.6:n.825-85A>T
ENST00000551114.2:n.728-85A>T
ENST00000553106.5:c.1066-85A>T	ENSP00000448059.1:n.1066-85A>T
ENST00000635477.1:c.170-85A>T
ENST00000635528.1:n.581-85A>T
NM_000277.1:c.1066-85A>T	NP_000268.1:n.1066-85A>T
XM_011538422.1:c.1009-85A>T	XP_011536724.1:n.1009-85A>T
NM_000277.2:c.1066-85A>T	NP_000268.1:n.1066-85A>T
NM_001354304.1:c.1066-85A>T	NP_001341233.1:n.1066-85A>T
NM_000277.3:c.1066-85A>T MANE Select	NP_000268.1:n.1066-85A>T
NM_001354304.2:c.1066-85A>T	NP_001341233.1:n.1066-85A>T