Canonical Allele Identifier: CA386303983
Gene: PAH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102894764T>C , CM000674.2:g.102894764T>C GRCh38
NC_000012.11:g.103288542T>C , CM000674.1:g.103288542T>C GRCh37
NC_000012.10:g.101812672T>C NCBI36
NG_008690.1:g.27839A>G
NG_008690.2:g.68647A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.323A>G MANE Select ENSP00000448059.1:p.Glu108Gly
ENST00000307000.7:c.308A>G ENSP00000303500.2:p.Glu103Gly
ENST00000546844.1:c.323A>G ENSP00000446658.1:p.Glu108Gly
ENST00000548928.1:n.245A>G
ENST00000549111.5:n.419A>G
ENST00000550978.6:c.307A>G
ENST00000551337.5:c.323A>G ENSP00000447620.1:p.Glu108Gly
ENST00000551988.5:n.412A>G
ENST00000553106.5:c.323A>G ENSP00000448059.1:p.Glu108Gly
NM_000277.1:c.323A>G NP_000268.1:p.Glu108Gly
XM_011538422.1:c.323A>G XP_011536724.1:p.Glu108Gly
NM_000277.2:c.323A>G NP_000268.1:p.Glu108Gly
NM_001354304.1:c.323A>G NP_001341233.1:p.Glu108Gly
XM_017019370.2:c.323A>G XP_016874859.1:p.Glu108Gly
NM_000277.3:c.323A>G MANE Select NP_000268.1:p.Glu108Gly
NM_001354304.2:c.323A>G NP_001341233.1:p.Glu108Gly