Canonical Allele Identifier: CA2620526618
Gene: PAH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102840262_102840263del , CM000674.2:g.102840262_102840263del GRCh38
NC_000012.11:g.103234040_103234041del , CM000674.1:g.103234040_103234041del GRCh37
NC_000012.10:g.101758170_101758171del NCBI36
NG_008690.1:g.82341_82342del
NG_008690.2:g.123149_123150del

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.1315+138_1315+139del MANE Select ENSP00000448059.1:n.1315+138_1315+139del
ENST00000307000.7:c.1300+138_1300+139del ENSP00000303500.2:n.1300+138_1300+139del
ENST00000551114.2:n.977+138_977+139del
ENST00000553106.5:c.1315+138_1315+139del ENSP00000448059.1:n.1315+138_1315+139del
ENST00000635477.1:c.419+138_419+139del
ENST00000635528.1:n.830+138_830+139del
NM_000277.1:c.1315+138_1315+139del NP_000268.1:n.1315+138_1315+139del
XM_011538422.1:c.1258+138_1258+139del XP_011536724.1:n.1258+138_1258+139del
NM_000277.2:c.1315+138_1315+139del NP_000268.1:n.1315+138_1315+139del
NM_001354304.1:c.1315+138_1315+139del NP_001341233.1:n.1315+138_1315+139del
NM_000277.3:c.1315+138_1315+139del MANE Select NP_000268.1:n.1315+138_1315+139del
NM_001354304.2:c.1315+138_1315+139del NP_001341233.1:n.1315+138_1315+139del