Canonical Allele Identifier: CA2059448260
Gene: PAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102854506T= , CM000674.2:g.102854506T= GRCh38
NC_000012.11:g.103248284T= , CM000674.1:g.103248284T= GRCh37
NC_000012.10:g.101772414T= NCBI36
NG_008690.1:g.68097A=
NG_008690.2:g.108905A=

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.706+630A= MANE Select ENSP00000448059.1:n.706+630A=
ENST00000307000.7:c.691+630A= ENSP00000303500.2:n.691+630A=
ENST00000553106.5:c.706+630A= ENSP00000448059.1:n.706+630A=
NM_000277.1:c.706+630A= NP_000268.1:n.706+630A=
XM_011538422.1:c.706+630A= XP_011536724.1:n.706+630A=
NM_000277.2:c.706+630A= NP_000268.1:n.706+630A=
NM_001354304.1:c.706+630A= NP_001341233.1:n.706+630A=
XM_017019370.2:c.*279A= XP_016874859.1:n.*279A=
NM_000277.3:c.706+630A= MANE Select NP_000268.1:n.706+630A=
NM_001354304.2:c.706+630A= NP_001341233.1:n.706+630A=