Canonical Allele Identifier: CA2059473262

Gene: PAH

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.102912793_102912795delinsCAA , CM000674.2:g.102912793_102912795delinsCAA	GRCh38
NC_000012.11:g.103306571_103306573delinsCAA , CM000674.1:g.103306571_103306573delinsCAA	GRCh37
NC_000012.10:g.101830701_101830703delinsCAA	NCBI36
NG_008690.1:g.9808_9810delinsTTG
NG_008690.2:g.50616_50618delinsTTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000553106.6:c.164_166delinsTTG MANE Select	ENSP00000448059.1:p.Phe55=
ENST00000307000.7:c.149_151delinsTTG	ENSP00000303500.2:p.Phe50=
ENST00000546844.1:c.164_166delinsTTG	ENSP00000446658.1:p.Phe55=
ENST00000548677.2:n.251_253delinsTTG
ENST00000548928.1:n.86_88delinsTTG
ENST00000549111.5:n.260_262delinsTTG
ENST00000550978.6:c.148_150delinsTTG
ENST00000551337.5:c.164_166delinsTTG	ENSP00000447620.1:p.Phe55=
ENST00000551988.5:n.253_255delinsTTG
ENST00000553106.5:c.164_166delinsTTG	ENSP00000448059.1:p.Phe55=
ENST00000635500.1:n.132_134delinsTTG
NM_000277.1:c.164_166delinsTTG	NP_000268.1:p.Phe55=
XM_011538422.1:c.164_166delinsTTG	XP_011536724.1:p.Phe55=
NM_000277.2:c.164_166delinsTTG	NP_000268.1:p.Phe55=
NM_001354304.1:c.164_166delinsTTG	NP_001341233.1:p.Phe55=
XM_017019370.2:c.164_166delinsTTG	XP_016874859.1:p.Phe55=
NM_000277.3:c.164_166delinsTTG MANE Select	NP_000268.1:p.Phe55=
NM_001354304.2:c.164_166delinsTTG	NP_001341233.1:p.Phe55=