Canonical Allele Identifier: CA2059448573
Gene: PAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102844432C= , CM000674.2:g.102844432C= GRCh38
NC_000012.11:g.103238210C= , CM000674.1:g.103238210C= GRCh37
NC_000012.10:g.101762340C= NCBI36
NG_008690.1:g.78171G=
NG_008690.2:g.118979G=

Transcript Alleles

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