Canonical Allele Identifier: CA2059447223
Gene: PAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102843933A= , CM000674.2:g.102843933A= GRCh38
NC_000012.11:g.103237711A= , CM000674.1:g.103237711A= GRCh37
NC_000012.10:g.101761841A= NCBI36
NG_008690.1:g.78670T=
NG_008690.2:g.119478T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.1066-154T= MANE Select ENSP00000448059.1:n.1066-154T=
ENST00000307000.7:c.1051-154T= ENSP00000303500.2:n.1051-154T=
ENST00000549247.6:n.825-154T=
ENST00000551114.2:n.728-154T=
ENST00000553106.5:c.1066-154T= ENSP00000448059.1:n.1066-154T=
ENST00000635477.1:c.170-154T=
ENST00000635528.1:n.581-154T=
NM_000277.1:c.1066-154T= NP_000268.1:n.1066-154T=
XM_011538422.1:c.1009-154T= XP_011536724.1:n.1009-154T=
NM_000277.2:c.1066-154T= NP_000268.1:n.1066-154T=
NM_001354304.1:c.1066-154T= NP_001341233.1:n.1066-154T=
NM_000277.3:c.1066-154T= MANE Select NP_000268.1:n.1066-154T=
NM_001354304.2:c.1066-154T= NP_001341233.1:n.1066-154T=