Canonical Allele Identifier: CA2575266775
Gene: PAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102844446del , CM000674.2:g.102844446del GRCh38
NC_000012.11:g.103238224del , CM000674.1:g.103238224del GRCh37
NC_000012.10:g.101762354del NCBI36
NG_008690.1:g.78157del
NG_008690.2:g.118965del

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.970-15del MANE Select ENSP00000448059.1:n.970-15del
ENST00000307000.7:c.955-15del ENSP00000303500.2:n.955-15del
ENST00000549247.6:n.729-15del
ENST00000551114.2:n.632-15del
ENST00000553106.5:c.970-15del ENSP00000448059.1:n.970-15del
ENST00000635477.1:c.74-15del
ENST00000635528.1:n.485-15del
NM_000277.1:c.970-15del NP_000268.1:n.970-15del
XM_011538422.1:c.913-15del XP_011536724.1:n.913-15del
NM_000277.2:c.970-15del NP_000268.1:n.970-15del
NM_001354304.1:c.970-15del NP_001341233.1:n.970-15del
NM_000277.3:c.970-15del MANE Select NP_000268.1:n.970-15del
NM_001354304.2:c.970-15del NP_001341233.1:n.970-15del