Canonical Allele Identifier: CA682806132
Gene: PAH HGNC NCBI

Linked Data

dbSNP Id: rs1202999063

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102854426_102854429del , CM000674.2:g.102854426_102854429del GRCh38
NC_000012.11:g.103248204_103248207del , CM000674.1:g.103248204_103248207del GRCh37
NC_000012.10:g.101772334_101772337del NCBI36
NG_008690.1:g.68177_68180del
NG_008690.2:g.108985_108988del

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.706+710_706+713del MANE Select ENSP00000448059.1:n.706+710_706+713del
ENST00000307000.7:c.691+710_691+713del ENSP00000303500.2:n.691+710_691+713del
ENST00000553106.5:c.706+710_706+713del ENSP00000448059.1:n.706+710_706+713del
NM_000277.1:c.706+710_706+713del NP_000268.1:n.706+710_706+713del
XM_011538422.1:c.706+710_706+713del XP_011536724.1:n.706+710_706+713del
NM_000277.2:c.706+710_706+713del NP_000268.1:n.706+710_706+713del
NM_001354304.1:c.706+710_706+713del NP_001341233.1:n.706+710_706+713del
XM_017019370.2:c.*359_*362del XP_016874859.1:n.*359_*362del
NM_000277.3:c.706+710_706+713del MANE Select NP_000268.1:n.706+710_706+713del
NM_001354304.2:c.706+710_706+713del NP_001341233.1:n.706+710_706+713del