Canonical Allele Identifier: CA2059441530
Gene: PAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102840425A= , CM000674.2:g.102840425A= GRCh38
NC_000012.11:g.103234203A= , CM000674.1:g.103234203A= GRCh37
NC_000012.10:g.101758333A= NCBI36
NG_008690.1:g.82178T=
NG_008690.2:g.122986T=

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.1290T= MANE Select ENSP00000448059.1:p.Leu430=
ENST00000307000.7:c.1275T= ENSP00000303500.2:p.Leu425=
ENST00000551114.2:n.952T=
ENST00000553106.5:c.1290T= ENSP00000448059.1:p.Leu430=
ENST00000635477.1:c.394T=
ENST00000635528.1:n.805T=
NM_000277.1:c.1290T= NP_000268.1:p.Leu430=
XM_011538422.1:c.1233T= XP_011536724.1:p.Leu411=
NM_000277.2:c.1290T= NP_000268.1:p.Leu430=
NM_001354304.1:c.1290T= NP_001341233.1:p.Leu430=
NM_000277.3:c.1290T= MANE Select NP_000268.1:p.Leu430=
NM_001354304.2:c.1290T= NP_001341233.1:p.Leu430=