Canonical Allele Identifier: CA386493391
Gene: PAH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102844343T>G , CM000674.2:g.102844343T>G GRCh38
NC_000012.11:g.103238121T>G , CM000674.1:g.103238121T>G GRCh37
NC_000012.10:g.101762251T>G NCBI36
NG_008690.1:g.78260A>C
NG_008690.2:g.119068A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.1058A>C MANE Select ENSP00000448059.1:p.Glu353Ala
ENST00000307000.7:c.1043A>C ENSP00000303500.2:p.Glu348Ala
ENST00000549247.6:n.817A>C
ENST00000551114.2:n.720A>C
ENST00000553106.5:c.1058A>C ENSP00000448059.1:p.Glu353Ala
ENST00000635477.1:c.162A>C
ENST00000635528.1:n.573A>C
NM_000277.1:c.1058A>C NP_000268.1:p.Glu353Ala
XM_011538422.1:c.1001A>C XP_011536724.1:p.Glu334Ala
NM_000277.2:c.1058A>C NP_000268.1:p.Glu353Ala
NM_001354304.1:c.1058A>C NP_001341233.1:p.Glu353Ala
NM_000277.3:c.1058A>C MANE Select NP_000268.1:p.Glu353Ala
NM_001354304.2:c.1058A>C NP_001341233.1:p.Glu353Ala