Canonical Allele Identifier: CA2059447658
Gene: PAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102844180_102844181delinsAA , CM000674.2:g.102844180_102844181delinsAA GRCh38
NC_000012.11:g.103237958_103237959delinsAA , CM000674.1:g.103237958_103237959delinsAA GRCh37
NC_000012.10:g.101762088_101762089delinsAA NCBI36
NG_008690.1:g.78422_78423delinsTT
NG_008690.2:g.119230_119231delinsTT

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.1065+155_1065+156delinsTT MANE Select ENSP00000448059.1:n.1065+155_1065+156deli...
ENST00000307000.7:c.1050+155_1050+156delinsTT ENSP00000303500.2:n.1050+155_1050+156deli...
ENST00000549247.6:n.824+155_824+156delinsTT
ENST00000551114.2:n.727+155_727+156delinsTT
ENST00000553106.5:c.1065+155_1065+156delinsTT ENSP00000448059.1:n.1065+155_1065+156deli...
ENST00000635477.1:c.169+155_169+156delinsTT
ENST00000635528.1:n.580+155_580+156delinsTT
NM_000277.1:c.1065+155_1065+156delinsTT NP_000268.1:n.1065+155_1065+156delinsTT
XM_011538422.1:c.1008+155_1008+156delinsTT XP_011536724.1:n.1008+155_1008+156delinsT...
NM_000277.2:c.1065+155_1065+156delinsTT NP_000268.1:n.1065+155_1065+156delinsTT
NM_001354304.1:c.1065+155_1065+156delinsTT NP_001341233.1:n.1065+155_1065+156delinsT...
NM_000277.3:c.1065+155_1065+156delinsTT MANE Select NP_000268.1:n.1065+155_1065+156delinsTT
NM_001354304.2:c.1065+155_1065+156delinsTT NP_001341233.1:n.1065+155_1065+156delinsT...