Canonical Allele Identifier: CA3194756526
Community Standard Title: NM_000277.3(PAH):c.605C= (p.Ala202=)
Gene: PAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102855237G= , CM000674.2:g.102855237G= GRCh38
NC_000012.11:g.103249015G= , CM000674.1:g.103249015G= GRCh37
NC_000012.10:g.101773145G= NCBI36
NG_008690.1:g.67366C=
NG_008690.2:g.108174C=

Transcript Alleles

HGVS Amino-acid Change
NM_000277.3:c.605C= MANE Select NP_000268.1:p.Ala202=
ENST00000553106.6:c.605C= MANE Select ENSP00000448059.1:p.Ala202=
NM_000277.1:c.605C= NP_000268.1:p.Ala202=
NM_000277.2:c.605C= NP_000268.1:p.Ala202=
NM_001354304.1:c.605C= NP_001341233.1:p.Ala202=
NM_001354304.2:c.605C= NP_001341233.1:p.Ala202=
ENST00000307000.7:c.590C= ENSP00000303500.2:p.Ala197=
ENST00000549111.5:n.701C=
ENST00000553106.5:c.605C= ENSP00000448059.1:p.Ala202=
XM_011538422.1:c.605C= XP_011536724.1:p.Ala202=
XM_017019370.2:c.605C= XP_016874859.1:p.Ala202=