Canonical Allele Identifier: CA386493517

Gene: PAH

Linked Data

• MyVariant Identifiers: chr12:g.103238203A>T (hg19) ; chr12:g.102844425A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.102844425A>T , CM000674.2:g.102844425A>T	GRCh38
NC_000012.11:g.103238203A>T , CM000674.1:g.103238203A>T	GRCh37
NC_000012.10:g.101762333A>T	NCBI36
NG_008690.1:g.78178T>A
NG_008690.2:g.118986T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553106.6:c.976T>A MANE Select	ENSP00000448059.1:p.Trp326Arg
ENST00000307000.7:c.961T>A	ENSP00000303500.2:p.Trp321Arg
ENST00000549247.6:n.735T>A
ENST00000551114.2:n.638T>A
ENST00000553106.5:c.976T>A	ENSP00000448059.1:p.Trp326Arg
ENST00000635477.1:c.80T>A
ENST00000635528.1:n.491T>A
NM_000277.1:c.976T>A	NP_000268.1:p.Trp326Arg
XM_011538422.1:c.919T>A	XP_011536724.1:p.Trp307Arg
NM_000277.2:c.976T>A	NP_000268.1:p.Trp326Arg
NM_001354304.1:c.976T>A	NP_001341233.1:p.Trp326Arg
NM_000277.3:c.976T>A MANE Select	NP_000268.1:p.Trp326Arg
NM_001354304.2:c.976T>A	NP_001341233.1:p.Trp326Arg