Canonical Allele Identifier: CA2059473665
Gene: PAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102913074A= , CM000674.2:g.102913074A= GRCh38
NC_000012.11:g.103306852A= , CM000674.1:g.103306852A= GRCh37
NC_000012.10:g.101830982A= NCBI36
NG_008690.1:g.9529T=
NG_008690.2:g.50337T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.61-176T= MANE Select ENSP00000448059.1:n.61-176T=
ENST00000307000.7:c.46-176T= ENSP00000303500.2:n.46-176T=
ENST00000546844.1:c.61-176T= ENSP00000446658.1:n.61-176T=
ENST00000548677.2:n.148-176T=
ENST00000549111.5:n.157-176T=
ENST00000550978.6:c.45-176T=
ENST00000551337.5:c.61-176T= ENSP00000447620.1:n.61-176T=
ENST00000551988.5:n.150-176T=
ENST00000553106.5:c.61-176T= ENSP00000448059.1:n.61-176T=
ENST00000635500.1:n.29-176T=
NM_000277.1:c.61-176T= NP_000268.1:n.61-176T=
XM_011538422.1:c.61-176T= XP_011536724.1:n.61-176T=
NM_000277.2:c.61-176T= NP_000268.1:n.61-176T=
NM_001354304.1:c.61-176T= NP_001341233.1:n.61-176T=
XM_017019370.2:c.61-176T= XP_016874859.1:n.61-176T=
NM_000277.3:c.61-176T= MANE Select NP_000268.1:n.61-176T=
NM_001354304.2:c.61-176T= NP_001341233.1:n.61-176T=