Canonical Allele Identifier: CA2059446076
Gene: PAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102843506G= , CM000674.2:g.102843506G= GRCh38
NC_000012.11:g.103237284G= , CM000674.1:g.103237284G= GRCh37
NC_000012.10:g.101761414G= NCBI36
NG_008690.1:g.79097C=
NG_008690.2:g.119905C=

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.1199+140C= MANE Select ENSP00000448059.1:n.1199+140C=
ENST00000307000.7:c.1184+140C= ENSP00000303500.2:n.1184+140C=
ENST00000549247.6:n.958+140C=
ENST00000551114.2:n.861+140C=
ENST00000553106.5:c.1199+140C= ENSP00000448059.1:n.1199+140C=
ENST00000635477.1:c.303+140C=
ENST00000635528.1:n.714+140C=
NM_000277.1:c.1199+140C= NP_000268.1:n.1199+140C=
XM_011538422.1:c.1142+140C= XP_011536724.1:n.1142+140C=
NM_000277.2:c.1199+140C= NP_000268.1:n.1199+140C=
NM_001354304.1:c.1199+140C= NP_001341233.1:n.1199+140C=
NM_000277.3:c.1199+140C= MANE Select NP_000268.1:n.1199+140C=
NM_001354304.2:c.1199+140C= NP_001341233.1:n.1199+140C=