Canonical Allele Identifier: CA386302198

Gene: PAH

Linked Data

• MyVariant Identifiers: chr12:g.103271289A>T (hg19) ; chr12:g.102877511A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.102877511A>T , CM000674.2:g.102877511A>T	GRCh38
NC_000012.11:g.103271289A>T , CM000674.1:g.103271289A>T	GRCh37
NC_000012.10:g.101795419A>T	NCBI36
NG_008690.1:g.45092T>A
NG_008690.2:g.85900T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000553106.6:c.392T>A MANE Select	ENSP00000448059.1:p.Phe131Tyr
ENST00000307000.7:c.377T>A	ENSP00000303500.2:p.Phe126Tyr
ENST00000549111.5:n.488T>A
ENST00000550978.6:c.376T>A
ENST00000551337.5:c.392T>A	ENSP00000447620.1:p.Phe131Tyr
ENST00000551988.5:n.481T>A
ENST00000553106.5:c.392T>A	ENSP00000448059.1:p.Phe131Tyr
NM_000277.1:c.392T>A	NP_000268.1:p.Phe131Tyr
XM_011538422.1:c.392T>A	XP_011536724.1:p.Phe131Tyr
NM_000277.2:c.392T>A	NP_000268.1:p.Phe131Tyr
NM_001354304.1:c.392T>A	NP_001341233.1:p.Phe131Tyr
XM_017019370.2:c.392T>A	XP_016874859.1:p.Phe131Tyr
NM_000277.3:c.392T>A MANE Select	NP_000268.1:p.Phe131Tyr
NM_001354304.2:c.392T>A	NP_001341233.1:p.Phe131Tyr