Canonical Allele Identifier: CA229807
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102865
ClinVar RCV Id: RCV000089126
dbSNP Id: rs199475668

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102852812_102852819del , CM000674.2:g.102852812_102852819del GRCh38
NC_000012.11:g.103246590_103246597del , CM000674.1:g.103246590_103246597del GRCh37
NC_000012.10:g.101770720_101770727del NCBI36
NG_008690.1:g.69784_69791del
NG_008690.2:g.110592_110599del

Transcript Alleles

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