Canonical Allele Identifier: CA386296572
Gene: PAH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102855157C>G , CM000674.2:g.102855157C>G GRCh38
NC_000012.11:g.103248935C>G , CM000674.1:g.103248935C>G GRCh37
NC_000012.10:g.101773065C>G NCBI36
NG_008690.1:g.67446G>C
NG_008690.2:g.108254G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.685G>C MANE Select ENSP00000448059.1:p.Asp229His
ENST00000307000.7:c.670G>C ENSP00000303500.2:p.Asp224His
ENST00000549111.5:n.781G>C
ENST00000553106.5:c.685G>C ENSP00000448059.1:p.Asp229His
NM_000277.1:c.685G>C NP_000268.1:p.Asp229His
XM_011538422.1:c.685G>C XP_011536724.1:p.Asp229His
NM_000277.2:c.685G>C NP_000268.1:p.Asp229His
NM_001354304.1:c.685G>C NP_001341233.1:p.Asp229His
XM_017019370.2:c.685G>C XP_016874859.1:p.Asp229His
NM_000277.3:c.685G>C MANE Select NP_000268.1:p.Asp229His
NM_001354304.2:c.685G>C NP_001341233.1:p.Asp229His