Canonical Allele Identifier: CA2536639652
Gene: PAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102844238del , CM000674.2:g.102844238del GRCh38
NC_000012.11:g.103238016del , CM000674.1:g.103238016del GRCh37
NC_000012.10:g.101762146del NCBI36
NG_008690.1:g.78368del
NG_008690.2:g.119176del

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.1065+101del MANE Select ENSP00000448059.1:n.1065+101del
ENST00000307000.7:c.1050+101del ENSP00000303500.2:n.1050+101del
ENST00000549247.6:n.824+101del
ENST00000551114.2:n.727+101del
ENST00000553106.5:c.1065+101del ENSP00000448059.1:n.1065+101del
ENST00000635477.1:c.169+101del
ENST00000635528.1:n.580+101del
NM_000277.1:c.1065+101del NP_000268.1:n.1065+101del
XM_011538422.1:c.1008+101del XP_011536724.1:n.1008+101del
NM_000277.2:c.1065+101del NP_000268.1:n.1065+101del
NM_001354304.1:c.1065+101del NP_001341233.1:n.1065+101del
NM_000277.3:c.1065+101del MANE Select NP_000268.1:n.1065+101del
NM_001354304.2:c.1065+101del NP_001341233.1:n.1065+101del