Canonical Allele Identifier: CA6748886
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 1157163
ClinVar RCV Id: RCV001500105
dbSNP Id: rs373782868

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102855200T>C , CM000674.2:g.102855200T>C GRCh38
NC_000012.11:g.103248978T>C , CM000674.1:g.103248978T>C GRCh37
NC_000012.10:g.101773108T>C NCBI36
NG_008690.1:g.67403A>G
NG_008690.2:g.108211A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.642A>G MANE Select ENSP00000448059.1:p.Glu214=
ENST00000307000.7:c.627A>G ENSP00000303500.2:p.Glu209=
ENST00000549111.5:n.738A>G
ENST00000553106.5:c.642A>G ENSP00000448059.1:p.Glu214=
NM_000277.1:c.642A>G NP_000268.1:p.Glu214=
XM_011538422.1:c.642A>G XP_011536724.1:p.Glu214=
NM_000277.2:c.642A>G NP_000268.1:p.Glu214=
NM_001354304.1:c.642A>G NP_001341233.1:p.Glu214=
XM_017019370.2:c.642A>G XP_016874859.1:p.Glu214=
NM_000277.3:c.642A>G MANE Select NP_000268.1:p.Glu214=
NM_001354304.2:c.642A>G NP_001341233.1:p.Glu214=