Canonical Allele Identifier: CA386493065
Gene: PAH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102840484A>C , CM000674.2:g.102840484A>C GRCh38
NC_000012.11:g.103234262A>C , CM000674.1:g.103234262A>C GRCh37
NC_000012.10:g.101758392A>C NCBI36
NG_008690.1:g.82119T>G
NG_008690.2:g.122927T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.1231T>G MANE Select ENSP00000448059.1:p.Ser411Ala
ENST00000307000.7:c.1216T>G ENSP00000303500.2:p.Ser406Ala
ENST00000551114.2:n.893T>G
ENST00000553106.5:c.1231T>G ENSP00000448059.1:p.Ser411Ala
ENST00000635477.1:c.335T>G
ENST00000635528.1:n.746T>G
NM_000277.1:c.1231T>G NP_000268.1:p.Ser411Ala
XM_011538422.1:c.1174T>G XP_011536724.1:p.Ser392Ala
NM_000277.2:c.1231T>G NP_000268.1:p.Ser411Ala
NM_001354304.1:c.1231T>G NP_001341233.1:p.Ser411Ala
NM_000277.3:c.1231T>G MANE Select NP_000268.1:p.Ser411Ala
NM_001354304.2:c.1231T>G NP_001341233.1:p.Ser411Ala