Canonical Allele Identifier: CA481331531
Gene: PAH HGNC NCBI

Linked Data

dbSNP Id: rs1320172123

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102852901C>A , CM000674.2:g.102852901C>A GRCh38
NC_000012.11:g.103246679C>A , CM000674.1:g.103246679C>A GRCh37
NC_000012.10:g.101770809C>A NCBI36
NG_008690.1:g.69702G>T
NG_008690.2:g.110510G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.756G>T MANE Select ENSP00000448059.1:p.Arg252=
ENST00000307000.7:c.741G>T ENSP00000303500.2:p.Arg247=
ENST00000549247.6:n.515G>T
ENST00000553106.5:c.756G>T ENSP00000448059.1:p.Arg252=
NM_000277.1:c.756G>T NP_000268.1:p.Arg252=
XM_011538422.1:c.756G>T XP_011536724.1:p.Arg252=
NM_000277.2:c.756G>T NP_000268.1:p.Arg252=
NM_001354304.1:c.756G>T NP_001341233.1:p.Arg252=
NM_000277.3:c.756G>T MANE Select NP_000268.1:p.Arg252=
NM_001354304.2:c.756G>T NP_001341233.1:p.Arg252=