Canonical Allele Identifier: CA2059442500
Gene: PAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102840743A= , CM000674.2:g.102840743A= GRCh38
NC_000012.11:g.103234521A= , CM000674.1:g.103234521A= GRCh37
NC_000012.10:g.101758651A= NCBI36
NG_008690.1:g.81860T=
NG_008690.2:g.122668T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.1200-228T= MANE Select ENSP00000448059.1:n.1200-228T=
ENST00000307000.7:c.1185-228T= ENSP00000303500.2:n.1185-228T=
ENST00000549247.6:n.959-228T=
ENST00000551114.2:n.862-228T=
ENST00000553106.5:c.1200-228T= ENSP00000448059.1:n.1200-228T=
ENST00000635477.1:c.304-228T=
ENST00000635528.1:n.715-228T=
NM_000277.1:c.1200-228T= NP_000268.1:n.1200-228T=
XM_011538422.1:c.1143-228T= XP_011536724.1:n.1143-228T=
NM_000277.2:c.1200-228T= NP_000268.1:n.1200-228T=
NM_001354304.1:c.1200-228T= NP_001341233.1:n.1200-228T=
NM_000277.3:c.1200-228T= MANE Select NP_000268.1:n.1200-228T=
NM_001354304.2:c.1200-228T= NP_001341233.1:n.1200-228T=