Canonical Allele Identifier: CA386492930
Gene: PAH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102840409A>C , CM000674.2:g.102840409A>C GRCh38
NC_000012.11:g.103234187A>C , CM000674.1:g.103234187A>C GRCh37
NC_000012.10:g.101758317A>C NCBI36
NG_008690.1:g.82194T>G
NG_008690.2:g.123002T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.1306T>G MANE Select ENSP00000448059.1:p.Ser436Ala
ENST00000307000.7:c.1291T>G ENSP00000303500.2:p.Ser431Ala
ENST00000551114.2:n.968T>G
ENST00000553106.5:c.1306T>G ENSP00000448059.1:p.Ser436Ala
ENST00000635477.1:n.410T>G
ENST00000635528.1:n.821T>G
NM_000277.1:c.1306T>G NP_000268.1:p.Ser436Ala
XM_011538422.1:c.1249T>G XP_011536724.1:p.Ser417Ala
NM_000277.2:c.1306T>G NP_000268.1:p.Ser436Ala
NM_001354304.1:c.1306T>G NP_001341233.1:p.Ser436Ala
NM_000277.3:c.1306T>G MANE Select NP_000268.1:p.Ser436Ala
NM_001354304.2:c.1306T>G NP_001341233.1:p.Ser436Ala