Canonical Allele Identifier: CA386296590
Gene: PAH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102855171A>C , CM000674.2:g.102855171A>C GRCh38
NC_000012.11:g.103248949A>C , CM000674.1:g.103248949A>C GRCh37
NC_000012.10:g.101773079A>C NCBI36
NG_008690.1:g.67432T>G
NG_008690.2:g.108240T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.671T>G MANE Select ENSP00000448059.1:p.Ile224Ser
ENST00000307000.7:c.656T>G ENSP00000303500.2:p.Ile219Ser
ENST00000549111.5:n.767T>G
ENST00000553106.5:c.671T>G ENSP00000448059.1:p.Ile224Ser
NM_000277.1:c.671T>G NP_000268.1:p.Ile224Ser
XM_011538422.1:c.671T>G XP_011536724.1:p.Ile224Ser
NM_000277.2:c.671T>G NP_000268.1:p.Ile224Ser
NM_001354304.1:c.671T>G NP_001341233.1:p.Ile224Ser
XM_017019370.2:c.671T>G XP_016874859.1:p.Ile224Ser
NM_000277.3:c.671T>G MANE Select NP_000268.1:p.Ile224Ser
NM_001354304.2:c.671T>G NP_001341233.1:p.Ile224Ser