Canonical Allele Identifier: CA6749060
Gene: PAH HGNC NCBI

Linked Data

dbSNP Id: rs771104344

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102917076C>G , CM000674.2:g.102917076C>G GRCh38
NC_000012.11:g.103310854C>G , CM000674.1:g.103310854C>G GRCh37
NC_000012.10:g.101834984C>G NCBI36
NG_008690.1:g.5527G>C
NG_008690.2:g.46335G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.55G>C MANE Select ENSP00000448059.1:p.Gly19Arg
ENST00000307000.7:c.-93G>C ENSP00000303500.2:n.-93G>C
ENST00000546844.1:c.55G>C ENSP00000446658.1:p.Gly19Arg
ENST00000547319.1:n.366G>C
ENST00000549111.5:n.151G>C
ENST00000550978.6:c.39G>C
ENST00000551337.5:c.55G>C ENSP00000447620.1:p.Gly19Arg
ENST00000551988.5:n.144G>C
ENST00000553106.5:c.55G>C ENSP00000448059.1:p.Gly19Arg
ENST00000635500.1:n.29-4178G>C
NM_000277.1:c.55G>C NP_000268.1:p.Gly19Arg
XM_011538422.1:c.55G>C XP_011536724.1:p.Gly19Arg
NM_000277.2:c.55G>C NP_000268.1:p.Gly19Arg
NM_001354304.1:c.55G>C NP_001341233.1:p.Gly19Arg
XM_017019370.2:c.55G>C XP_016874859.1:p.Gly19Arg
NM_000277.3:c.55G>C MANE Select NP_000268.1:p.Gly19Arg
NM_001354304.2:c.55G>C NP_001341233.1:p.Gly19Arg