Canonical Allele Identifier: CA2059445979
Gene: PAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102852811_102852819delinsTCACGGTTC , CM000674.2:g.102852811_102852819delinsTCACGGTTC GRCh38
NC_000012.11:g.103246589_103246597delinsTCACGGTTC , CM000674.1:g.103246589_103246597delinsTCACGGTTC GRCh37
NC_000012.10:g.101770719_101770727delinsTCACGGTTC NCBI36
NG_008690.1:g.69784_69792delinsGAACCGTGA
NG_008690.2:g.110592_110600delinsGAACCGTGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.838_842+4delinsGAACCGTGA
ENST00000307000.7:c.823_827+4delinsGAACCGTGA
ENST00000549247.6:n.597_601+4delinsGAACCGTGA
ENST00000553106.5:c.838_842+4delinsGAACCGTGA
NM_000277.1:c.838_842+4delinsGAACCGTGA
XM_011538422.1:c.838_842+4delinsGAACCGTGA
NM_000277.2:c.838_842+4delinsGAACCGTGA
NM_001354304.1:c.838_842+4delinsGAACCGTGA
NM_000277.3:c.838_842+4delinsGAACCGTGA
NM_001354304.2:c.838_842+4delinsGAACCGTGA