Canonical Allele Identifier: CA2059446528
Gene: PAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102843691A= , CM000674.2:g.102843691A= GRCh38
NC_000012.11:g.103237469A= , CM000674.1:g.103237469A= GRCh37
NC_000012.10:g.101761599A= NCBI36
NG_008690.1:g.78912T=
NG_008690.2:g.119720T=

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.1154T= MANE Select ENSP00000448059.1:p.Leu385=
ENST00000307000.7:c.1139T= ENSP00000303500.2:p.Leu380=
ENST00000549247.6:n.913T=
ENST00000551114.2:n.816T=
ENST00000553106.5:c.1154T= ENSP00000448059.1:p.Leu385=
ENST00000635477.1:c.258T=
ENST00000635528.1:n.669T=
NM_000277.1:c.1154T= NP_000268.1:p.Leu385=
XM_011538422.1:c.1097T= XP_011536724.1:p.Leu366=
NM_000277.2:c.1154T= NP_000268.1:p.Leu385=
NM_001354304.1:c.1154T= NP_001341233.1:p.Leu385=
NM_000277.3:c.1154T= MANE Select NP_000268.1:p.Leu385=
NM_001354304.2:c.1154T= NP_001341233.1:p.Leu385=