Canonical Allele Identifier: CA2059449676
Gene: PAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102855282_102855284delinsCAT , CM000674.2:g.102855282_102855284delinsCAT GRCh38
NC_000012.11:g.103249060_103249062delinsCAT , CM000674.1:g.103249060_103249062delinsCAT GRCh37
NC_000012.10:g.101773190_101773192delinsCAT NCBI36
NG_008690.1:g.67319_67321delinsATG
NG_008690.2:g.108127_108129delinsATG

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.558_560delinsATG MANE Select ENSP00000448059.1:p.Thr186=
ENST00000307000.7:c.543_545delinsATG ENSP00000303500.2:p.Thr181=
ENST00000549111.5:n.654_656delinsATG
ENST00000551988.5:n.579_581delinsATG
ENST00000553106.5:c.558_560delinsATG ENSP00000448059.1:p.Thr186=
NM_000277.1:c.558_560delinsATG NP_000268.1:p.Thr186=
XM_011538422.1:c.558_560delinsATG XP_011536724.1:p.Thr186=
NM_000277.2:c.558_560delinsATG NP_000268.1:p.Thr186=
NM_001354304.1:c.558_560delinsATG NP_001341233.1:p.Thr186=
XM_017019370.2:c.558_560delinsATG XP_016874859.1:p.Thr186=
NM_000277.3:c.558_560delinsATG MANE Select NP_000268.1:p.Thr186=
NM_001354304.2:c.558_560delinsATG NP_001341233.1:p.Thr186=