Canonical Allele Identifier: CA386299516
Gene: PAH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102866614A>C , CM000674.2:g.102866614A>C GRCh38
NC_000012.11:g.103260392A>C , CM000674.1:g.103260392A>C GRCh37
NC_000012.10:g.101784522A>C NCBI36
NG_008690.1:g.55989T>G
NG_008690.2:g.96797T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.491T>G MANE Select ENSP00000448059.1:p.Ile164Ser
ENST00000307000.7:c.476T>G ENSP00000303500.2:p.Ile159Ser
ENST00000549111.5:n.587T>G
ENST00000551988.5:n.530+10848T>G
ENST00000553106.5:c.491T>G ENSP00000448059.1:p.Ile164Ser
NM_000277.1:c.491T>G NP_000268.1:p.Ile164Ser
XM_011538422.1:c.491T>G XP_011536724.1:p.Ile164Ser
NM_000277.2:c.491T>G NP_000268.1:p.Ile164Ser
NM_001354304.1:c.491T>G NP_001341233.1:p.Ile164Ser
XM_017019370.2:c.491T>G XP_016874859.1:p.Ile164Ser
NM_000277.3:c.491T>G MANE Select NP_000268.1:p.Ile164Ser
NM_001354304.2:c.491T>G NP_001341233.1:p.Ile164Ser