Canonical Allele Identifier: CA2059448173
Gene: PAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102854419T= , CM000674.2:g.102854419T= GRCh38
NC_000012.11:g.103248197T= , CM000674.1:g.103248197T= GRCh37
NC_000012.10:g.101772327T= NCBI36
NG_008690.1:g.68184A=
NG_008690.2:g.108992A=

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.706+717A= MANE Select ENSP00000448059.1:n.706+717A=
ENST00000307000.7:c.691+717A= ENSP00000303500.2:n.691+717A=
ENST00000553106.5:c.706+717A= ENSP00000448059.1:n.706+717A=
NM_000277.1:c.706+717A= NP_000268.1:n.706+717A=
XM_011538422.1:c.706+717A= XP_011536724.1:n.706+717A=
NM_000277.2:c.706+717A= NP_000268.1:n.706+717A=
NM_001354304.1:c.706+717A= NP_001341233.1:n.706+717A=
XM_017019370.2:c.*366A= XP_016874859.1:n.*366A=
NM_000277.3:c.706+717A= MANE Select NP_000268.1:n.706+717A=
NM_001354304.2:c.706+717A= NP_001341233.1:n.706+717A=