Canonical Allele Identifier: CA229394
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102564
dbSNP Id: rs63186960

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102840516del , CM000674.2:g.102840516del GRCh38
NC_000012.11:g.103234294del , CM000674.1:g.103234294del GRCh37
NC_000012.10:g.101758424del NCBI36
NG_008690.1:g.82088del
NG_008690.2:g.122896del

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.1200del
ENST00000307000.7:c.1185del
ENST00000549247.6:n.959del
ENST00000551114.2:n.862del
ENST00000553106.5:c.1200del
ENST00000635477.1:c.304del
ENST00000635528.1:n.715del
NM_000277.1:c.1200del
XM_011538422.1:c.1143del
NM_000277.2:c.1200del
NM_001354304.1:c.1200del
NM_000277.3:c.1200del
NM_001354304.2:c.1200del