Canonical Allele Identifier: CA386299523
Gene: PAH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102866615T>G , CM000674.2:g.102866615T>G GRCh38
NC_000012.11:g.103260393T>G , CM000674.1:g.103260393T>G GRCh37
NC_000012.10:g.101784523T>G NCBI36
NG_008690.1:g.55988A>C
NG_008690.2:g.96796A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.490A>C MANE Select ENSP00000448059.1:p.Ile164Leu
ENST00000307000.7:c.475A>C ENSP00000303500.2:p.Ile159Leu
ENST00000549111.5:n.586A>C
ENST00000551988.5:n.530+10847A>C
ENST00000553106.5:c.490A>C ENSP00000448059.1:p.Ile164Leu
NM_000277.1:c.490A>C NP_000268.1:p.Ile164Leu
XM_011538422.1:c.490A>C XP_011536724.1:p.Ile164Leu
NM_000277.2:c.490A>C NP_000268.1:p.Ile164Leu
NM_001354304.1:c.490A>C NP_001341233.1:p.Ile164Leu
XM_017019370.2:c.490A>C XP_016874859.1:p.Ile164Leu
NM_000277.3:c.490A>C MANE Select NP_000268.1:p.Ile164Leu
NM_001354304.2:c.490A>C NP_001341233.1:p.Ile164Leu