Canonical Allele Identifier: CA2059451395
Gene: PAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102846928A= , CM000674.2:g.102846928A= GRCh38
NC_000012.11:g.103240706A= , CM000674.1:g.103240706A= GRCh37
NC_000012.10:g.101764836A= NCBI36
NG_008690.1:g.75675T=
NG_008690.2:g.116483T=

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.936T= MANE Select ENSP00000448059.1:p.Gly312=
ENST00000307000.7:c.921T= ENSP00000303500.2:p.Gly307=
ENST00000549247.6:n.695T=
ENST00000551114.2:n.598T=
ENST00000553106.5:c.936T= ENSP00000448059.1:p.Gly312=
ENST00000635477.1:c.74-2497T=
ENST00000635528.1:n.451T=
NM_000277.1:c.936T= NP_000268.1:p.Gly312=
XM_011538422.1:c.913-2497T= XP_011536724.1:n.913-2497T=
NM_000277.2:c.936T= NP_000268.1:p.Gly312=
NM_001354304.1:c.936T= NP_001341233.1:p.Gly312=
NM_000277.3:c.936T= MANE Select NP_000268.1:p.Gly312=
NM_001354304.2:c.936T= NP_001341233.1:p.Gly312=