Canonical Allele Identifier: CA386291576
Gene: PAH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102846908T>G , CM000674.2:g.102846908T>G GRCh38
NC_000012.11:g.103240686T>G , CM000674.1:g.103240686T>G GRCh37
NC_000012.10:g.101764816T>G NCBI36
NG_008690.1:g.75695A>C
NG_008690.2:g.116503A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.956A>C MANE Select ENSP00000448059.1:p.Glu319Ala
ENST00000307000.7:c.941A>C ENSP00000303500.2:p.Glu314Ala
ENST00000549247.6:n.715A>C
ENST00000551114.2:n.618A>C
ENST00000553106.5:c.956A>C ENSP00000448059.1:p.Glu319Ala
ENST00000635477.1:n.74-2477A>C
ENST00000635528.1:n.471A>C
NM_000277.1:c.956A>C NP_000268.1:p.Glu319Ala
XM_011538422.1:c.913-2477A>C XP_011536724.1:n.913-2477A>C
NM_000277.2:c.956A>C NP_000268.1:p.Glu319Ala
NM_001354304.1:c.956A>C NP_001341233.1:p.Glu319Ala
NM_000277.3:c.956A>C MANE Select NP_000268.1:p.Glu319Ala
NM_001354304.2:c.956A>C NP_001341233.1:p.Glu319Ala