Canonical Allele Identifier: CA2059443789
Gene: PAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102851259G= , CM000674.2:g.102851259G= GRCh38
NC_000012.11:g.103245037G= , CM000674.1:g.103245037G= GRCh37
NC_000012.10:g.101769167G= NCBI36
NG_008690.1:g.71344C=
NG_008690.2:g.112152C=

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.912+428C= MANE Select ENSP00000448059.1:n.912+428C=
ENST00000307000.7:c.897+428C= ENSP00000303500.2:n.897+428C=
ENST00000549247.6:n.671+428C=
ENST00000551114.2:n.574+428C=
ENST00000553106.5:c.912+428C= ENSP00000448059.1:n.912+428C=
ENST00000635477.1:c.73+428C=
NM_000277.1:c.912+428C= NP_000268.1:n.912+428C=
XM_011538422.1:c.912+428C= XP_011536724.1:n.912+428C=
NM_000277.2:c.912+428C= NP_000268.1:n.912+428C=
NM_001354304.1:c.912+428C= NP_001341233.1:n.912+428C=
NM_000277.3:c.912+428C= MANE Select NP_000268.1:n.912+428C=
NM_001354304.2:c.912+428C= NP_001341233.1:n.912+428C=