Canonical Allele Identifier: CA2059441765
Gene: PAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102840469G= , CM000674.2:g.102840469G= GRCh38
NC_000012.11:g.103234247G= , CM000674.1:g.103234247G= GRCh37
NC_000012.10:g.101758377G= NCBI36
NG_008690.1:g.82134C=
NG_008690.2:g.122942C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.1246C= MANE Select ENSP00000448059.1:p.Pro416=
ENST00000307000.7:c.1231C= ENSP00000303500.2:p.Pro411=
ENST00000551114.2:n.908C=
ENST00000553106.5:c.1246C= ENSP00000448059.1:p.Pro416=
ENST00000635477.1:c.350C=
ENST00000635528.1:n.761C=
NM_000277.1:c.1246C= NP_000268.1:p.Pro416=
XM_011538422.1:c.1189C= XP_011536724.1:p.Pro397=
NM_000277.2:c.1246C= NP_000268.1:p.Pro416=
NM_001354304.1:c.1246C= NP_001341233.1:p.Pro416=
NM_000277.3:c.1246C= MANE Select NP_000268.1:p.Pro416=
NM_001354304.2:c.1246C= NP_001341233.1:p.Pro416=