Canonical Allele Identifier: CA2059451470
Gene: PAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102846942G= , CM000674.2:g.102846942G= GRCh38
NC_000012.11:g.103240720G= , CM000674.1:g.103240720G= GRCh37
NC_000012.10:g.101764850G= NCBI36
NG_008690.1:g.75661C=
NG_008690.2:g.116469C=

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.922C= MANE Select ENSP00000448059.1:p.Leu308=
ENST00000307000.7:c.907C= ENSP00000303500.2:p.Leu303=
ENST00000549247.6:n.681C=
ENST00000551114.2:n.584C=
ENST00000553106.5:c.922C= ENSP00000448059.1:p.Leu308=
ENST00000635477.1:c.74-2511C=
ENST00000635528.1:n.437C=
NM_000277.1:c.922C= NP_000268.1:p.Leu308=
XM_011538422.1:c.913-2511C= XP_011536724.1:n.913-2511C=
NM_000277.2:c.922C= NP_000268.1:p.Leu308=
NM_001354304.1:c.922C= NP_001341233.1:p.Leu308=
NM_000277.3:c.922C= MANE Select NP_000268.1:p.Leu308=
NM_001354304.2:c.922C= NP_001341233.1:p.Leu308=