Canonical Allele Identifier: CA2620511367
Gene: PAH HGNC NCBI

Linked Data

gnomAD v4: 12-102851597-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102851597A>G , CM000674.2:g.102851597A>G GRCh38
NC_000012.11:g.103245375A>G , CM000674.1:g.103245375A>G GRCh37
NC_000012.10:g.101769505A>G NCBI36
NG_008690.1:g.71006T>C
NG_008690.2:g.111814T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.912+90T>C MANE Select ENSP00000448059.1:n.912+90T>C
ENST00000307000.7:c.897+90T>C ENSP00000303500.2:n.897+90T>C
ENST00000549247.6:n.671+90T>C
ENST00000551114.2:n.574+90T>C
ENST00000553106.5:c.912+90T>C ENSP00000448059.1:n.912+90T>C
ENST00000635477.1:c.73+90T>C
NM_000277.1:c.912+90T>C NP_000268.1:n.912+90T>C
XM_011538422.1:c.912+90T>C XP_011536724.1:n.912+90T>C
NM_000277.2:c.912+90T>C NP_000268.1:n.912+90T>C
NM_001354304.1:c.912+90T>C NP_001341233.1:n.912+90T>C
NM_000277.3:c.912+90T>C MANE Select NP_000268.1:n.912+90T>C
NM_001354304.2:c.912+90T>C NP_001341233.1:n.912+90T>C
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