Canonical Allele Identifier: CA2513917382

Gene: PAH

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.102852778T>A , CM000674.2:g.102852778T>A	GRCh38
NC_000012.11:g.103246556T>A , CM000674.1:g.103246556T>A	GRCh37
NC_000012.10:g.101770686T>A	NCBI36
NG_008690.1:g.69825A>T
NG_008690.2:g.110633A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000553106.6:c.842+37A>T MANE Select	ENSP00000448059.1:n.842+37A>T
ENST00000307000.7:c.827+37A>T	ENSP00000303500.2:n.827+37A>T
ENST00000549247.6:n.601+37A>T
ENST00000553106.5:c.842+37A>T	ENSP00000448059.1:n.842+37A>T
ENST00000635477.1:c.3+37A>T
NM_000277.1:c.842+37A>T	NP_000268.1:n.842+37A>T
XM_011538422.1:c.842+37A>T	XP_011536724.1:n.842+37A>T
NM_000277.2:c.842+37A>T	NP_000268.1:n.842+37A>T
NM_001354304.1:c.842+37A>T	NP_001341233.1:n.842+37A>T
NM_000277.3:c.842+37A>T MANE Select	NP_000268.1:n.842+37A>T
NM_001354304.2:c.842+37A>T	NP_001341233.1:n.842+37A>T