Canonical Allele Identifier: CA2059476053
Gene: PAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102916860C= , CM000674.2:g.102916860C= GRCh38
NC_000012.11:g.103310638C= , CM000674.1:g.103310638C= GRCh37
NC_000012.10:g.101834768C= NCBI36
NG_008690.1:g.5743G=
NG_008690.2:g.46551G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.60+211G= MANE Select ENSP00000448059.1:n.60+211G=
ENST00000307000.7:c.-88+211G= ENSP00000303500.2:n.-88+211G=
ENST00000546844.1:c.60+211G= ENSP00000446658.1:n.60+211G=
ENST00000547319.1:n.371+211G=
ENST00000549111.5:n.156+211G=
ENST00000550978.6:c.44+211G=
ENST00000551337.5:c.60+211G= ENSP00000447620.1:n.60+211G=
ENST00000551988.5:n.149+211G=
ENST00000553106.5:c.60+211G= ENSP00000448059.1:n.60+211G=
ENST00000635500.1:n.29-3962G=
NM_000277.1:c.60+211G= NP_000268.1:n.60+211G=
XM_011538422.1:c.60+211G= XP_011536724.1:n.60+211G=
NM_000277.2:c.60+211G= NP_000268.1:n.60+211G=
NM_001354304.1:c.60+211G= NP_001341233.1:n.60+211G=
XM_017019370.2:c.60+211G= XP_016874859.1:n.60+211G=
NM_000277.3:c.60+211G= MANE Select NP_000268.1:n.60+211G=
NM_001354304.2:c.60+211G= NP_001341233.1:n.60+211G=