Canonical Allele Identifier: CA2059448919
Gene: PAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102844623G= , CM000674.2:g.102844623G= GRCh38
NC_000012.11:g.103238401G= , CM000674.1:g.103238401G= GRCh37
NC_000012.10:g.101762531G= NCBI36
NG_008690.1:g.77980C=
NG_008690.2:g.118788C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.970-192C= MANE Select ENSP00000448059.1:n.970-192C=
ENST00000307000.7:c.955-192C= ENSP00000303500.2:n.955-192C=
ENST00000549247.6:n.729-192C=
ENST00000551114.2:n.632-192C=
ENST00000553106.5:c.970-192C= ENSP00000448059.1:n.970-192C=
ENST00000635477.1:c.74-192C=
ENST00000635528.1:n.485-192C=
NM_000277.1:c.970-192C= NP_000268.1:n.970-192C=
XM_011538422.1:c.913-192C= XP_011536724.1:n.913-192C=
NM_000277.2:c.970-192C= NP_000268.1:n.970-192C=
NM_001354304.1:c.970-192C= NP_001341233.1:n.970-192C=
NM_000277.3:c.970-192C= MANE Select NP_000268.1:n.970-192C=
NM_001354304.2:c.970-192C= NP_001341233.1:n.970-192C=