Canonical Allele Identifier: CA16020897
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 1065385
ClinVar RCV Id: RCV001375905
dbSNP Id: rs2136639687

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102846945del , CM000674.2:g.102846945del GRCh38
NC_000012.11:g.103240723del , CM000674.1:g.103240723del GRCh37
NC_000012.10:g.101764853del NCBI36
NG_008690.1:g.75659del
NG_008690.2:g.116467del

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.920del MANE Select ENSP00000448059.1:p.Gly307AlafsTer?
ENST00000307000.7:c.905del ENSP00000303500.2:p.Gly302AlafsTer?
ENST00000549247.6:n.679del
ENST00000551114.2:n.582del
ENST00000553106.5:c.920del ENSP00000448059.1:p.Gly307AlafsTer?
ENST00000635477.1:c.74-2513del
ENST00000635528.1:n.435del
NM_000277.1:c.920del NP_000268.1:p.Gly307AlafsTer?
XM_011538422.1:c.913-2513del XP_011536724.1:n.913-2513del
NM_000277.2:c.920del NP_000268.1:p.Gly307AlafsTer?
NM_001354304.1:c.920del NP_001341233.1:p.Gly307AlafsTer?
NM_000277.3:c.920del MANE Select NP_000268.1:p.Gly307AlafsTer?
NM_001354304.2:c.920del NP_001341233.1:p.Gly307AlafsTer?