Canonical Allele Identifier: CA16020782
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 872833
ClinVar RCV Id: RCV001093505
dbSNP Id: rs1876625601

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102877523T>C , CM000674.2:g.102877523T>C GRCh38
NC_000012.11:g.103271301T>C , CM000674.1:g.103271301T>C GRCh37
NC_000012.10:g.101795431T>C NCBI36
NG_008690.1:g.45080A>G
NG_008690.2:g.85888A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.380A>G MANE Select ENSP00000448059.1:p.Glu127Gly
ENST00000307000.7:c.365A>G ENSP00000303500.2:p.Glu122Gly
ENST00000549111.5:n.476A>G
ENST00000550978.6:c.364A>G
ENST00000551337.5:c.380A>G ENSP00000447620.1:p.Glu127Gly
ENST00000551988.5:n.469A>G
ENST00000553106.5:c.380A>G ENSP00000448059.1:p.Glu127Gly
NM_000277.1:c.380A>G NP_000268.1:p.Glu127Gly
XM_011538422.1:c.380A>G XP_011536724.1:p.Glu127Gly
NM_000277.2:c.380A>G NP_000268.1:p.Glu127Gly
NM_001354304.1:c.380A>G NP_001341233.1:p.Glu127Gly
XM_017019370.2:c.380A>G XP_016874859.1:p.Glu127Gly
NM_000277.3:c.380A>G MANE Select NP_000268.1:p.Glu127Gly
NM_001354304.2:c.380A>G NP_001341233.1:p.Glu127Gly