Canonical Allele Identifier: CA386296623
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 1754238
dbSNP Id: rs1164279708

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102855186A>T , CM000674.2:g.102855186A>T GRCh38
NC_000012.11:g.103248964A>T , CM000674.1:g.103248964A>T GRCh37
NC_000012.10:g.101773094A>T NCBI36
NG_008690.1:g.67417T>A
NG_008690.2:g.108225T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.656T>A MANE Select ENSP00000448059.1:p.Phe219Tyr
ENST00000307000.7:c.641T>A ENSP00000303500.2:p.Phe214Tyr
ENST00000549111.5:n.752T>A
ENST00000553106.5:c.656T>A ENSP00000448059.1:p.Phe219Tyr
NM_000277.1:c.656T>A NP_000268.1:p.Phe219Tyr
XM_011538422.1:c.656T>A XP_011536724.1:p.Phe219Tyr
NM_000277.2:c.656T>A NP_000268.1:p.Phe219Tyr
NM_001354304.1:c.656T>A NP_001341233.1:p.Phe219Tyr
XM_017019370.2:c.656T>A XP_016874859.1:p.Phe219Tyr
NM_000277.3:c.656T>A MANE Select NP_000268.1:p.Phe219Tyr
NM_001354304.2:c.656T>A NP_001341233.1:p.Phe219Tyr