Canonical Allele Identifier: CA951234472
Gene: PAH HGNC NCBI

Linked Data

dbSNP Id: rs1875123818

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102851066del , CM000674.2:g.102851066del GRCh38
NC_000012.11:g.103244844del , CM000674.1:g.103244844del GRCh37
NC_000012.10:g.101768974del NCBI36
NG_008690.1:g.71539del
NG_008690.2:g.112347del

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.912+623del MANE Select ENSP00000448059.1:n.912+623del
ENST00000307000.7:c.897+623del ENSP00000303500.2:n.897+623del
ENST00000549247.6:n.671+623del
ENST00000551114.2:n.574+623del
ENST00000553106.5:c.912+623del ENSP00000448059.1:n.912+623del
ENST00000635477.1:c.73+623del
NM_000277.1:c.912+623del NP_000268.1:n.912+623del
XM_011538422.1:c.912+623del XP_011536724.1:n.912+623del
NM_000277.2:c.912+623del NP_000268.1:n.912+623del
NM_001354304.1:c.912+623del NP_001341233.1:n.912+623del
NM_000277.3:c.912+623del MANE Select NP_000268.1:n.912+623del
NM_001354304.2:c.912+623del NP_001341233.1:n.912+623del