Canonical Allele Identifier: CA2059448541
Gene: PAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102854814C= , CM000674.2:g.102854814C= GRCh38
NC_000012.11:g.103248592C= , CM000674.1:g.103248592C= GRCh37
NC_000012.10:g.101772722C= NCBI36
NG_008690.1:g.67789G=
NG_008690.2:g.108597G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.706+322G= MANE Select ENSP00000448059.1:n.706+322G=
ENST00000307000.7:c.691+322G= ENSP00000303500.2:n.691+322G=
ENST00000549111.5:n.1124G=
ENST00000553106.5:c.706+322G= ENSP00000448059.1:n.706+322G=
NM_000277.1:c.706+322G= NP_000268.1:n.706+322G=
XM_011538422.1:c.706+322G= XP_011536724.1:n.706+322G=
NM_000277.2:c.706+322G= NP_000268.1:n.706+322G=
NM_001354304.1:c.706+322G= NP_001341233.1:n.706+322G=
XM_017019370.2:c.707-13G= XP_016874859.1:n.707-13G=
NM_000277.3:c.706+322G= MANE Select NP_000268.1:n.706+322G=
NM_001354304.2:c.706+322G= NP_001341233.1:n.706+322G=