Canonical Allele Identifier: CA386304090
Gene: PAH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102894818G>T , CM000674.2:g.102894818G>T GRCh38
NC_000012.11:g.103288596G>T , CM000674.1:g.103288596G>T GRCh37
NC_000012.10:g.101812726G>T NCBI36
NG_008690.1:g.27785C>A
NG_008690.2:g.68593C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.269C>A MANE Select ENSP00000448059.1:p.Ala90Asp
ENST00000307000.7:c.254C>A ENSP00000303500.2:p.Ala85Asp
ENST00000546844.1:c.269C>A ENSP00000446658.1:p.Ala90Asp
ENST00000548677.2:n.356C>A
ENST00000548928.1:n.191C>A
ENST00000549111.5:n.365C>A
ENST00000550978.6:c.253C>A
ENST00000551337.5:c.269C>A ENSP00000447620.1:p.Ala90Asp
ENST00000551988.5:n.358C>A
ENST00000553106.5:c.269C>A ENSP00000448059.1:p.Ala90Asp
NM_000277.1:c.269C>A NP_000268.1:p.Ala90Asp
XM_011538422.1:c.269C>A XP_011536724.1:p.Ala90Asp
NM_000277.2:c.269C>A NP_000268.1:p.Ala90Asp
NM_001354304.1:c.269C>A NP_001341233.1:p.Ala90Asp
XM_017019370.2:c.269C>A XP_016874859.1:p.Ala90Asp
NM_000277.3:c.269C>A MANE Select NP_000268.1:p.Ala90Asp
NM_001354304.2:c.269C>A NP_001341233.1:p.Ala90Asp