Canonical Allele Identifier: CA229598
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102716
dbSNP Id: rs199475613

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102855331C>T , CM000674.2:g.102855331C>T GRCh38
NC_000012.11:g.103249109C>T , CM000674.1:g.103249109C>T GRCh37
NC_000012.10:g.101773239C>T NCBI36
NG_008690.1:g.67272G>A
NG_008690.2:g.108080G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.511G>A MANE Select ENSP00000448059.1:p.Gly171Arg
ENST00000307000.7:c.496G>A ENSP00000303500.2:p.Gly166Arg
ENST00000549111.5:n.607G>A
ENST00000551988.5:n.532G>A
ENST00000553106.5:c.511G>A ENSP00000448059.1:p.Gly171Arg
NM_000277.1:c.511G>A NP_000268.1:p.Gly171Arg
XM_011538422.1:c.511G>A XP_011536724.1:p.Gly171Arg
NM_000277.2:c.511G>A NP_000268.1:p.Gly171Arg
NM_001354304.1:c.511G>A NP_001341233.1:p.Gly171Arg
XM_017019370.2:c.511G>A XP_016874859.1:p.Gly171Arg
NM_000277.3:c.511G>A MANE Select NP_000268.1:p.Gly171Arg
NM_001354304.2:c.511G>A NP_001341233.1:p.Gly171Arg