Canonical Allele Identifier: CA2059446819
Gene: PAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102852975C= , CM000674.2:g.102852975C= GRCh38
NC_000012.11:g.103246753C= , CM000674.1:g.103246753C= GRCh37
NC_000012.10:g.101770883C= NCBI36
NG_008690.1:g.69628G=
NG_008690.2:g.110436G=

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.707-25G= MANE Select ENSP00000448059.1:n.707-25G=
ENST00000307000.7:c.692-25G= ENSP00000303500.2:n.692-25G=
ENST00000549247.6:n.441G=
ENST00000553106.5:c.707-25G= ENSP00000448059.1:n.707-25G=
NM_000277.1:c.707-25G= NP_000268.1:n.707-25G=
XM_011538422.1:c.707-25G= XP_011536724.1:n.707-25G=
NM_000277.2:c.707-25G= NP_000268.1:n.707-25G=
NM_001354304.1:c.707-25G= NP_001341233.1:n.707-25G=
NM_000277.3:c.707-25G= MANE Select NP_000268.1:n.707-25G=
NM_001354304.2:c.707-25G= NP_001341233.1:n.707-25G=