Canonical Allele Identifier: CA2620507643
Gene: PAH HGNC NCBI

Linked Data

gnomAD v4: 12-102894700-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102894700A>T , CM000674.2:g.102894700A>T GRCh38
NC_000012.11:g.103288478A>T , CM000674.1:g.103288478A>T GRCh37
NC_000012.10:g.101812608A>T NCBI36
NG_008690.1:g.27903T>A
NG_008690.2:g.68711T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.352+35T>A MANE Select ENSP00000448059.1:n.352+35T>A
ENST00000307000.7:c.337+35T>A ENSP00000303500.2:n.337+35T>A
ENST00000548928.1:n.274+35T>A
ENST00000549111.5:n.448+35T>A
ENST00000550978.6:c.336+35T>A
ENST00000551337.5:c.352+35T>A ENSP00000447620.1:n.352+35T>A
ENST00000551988.5:n.441+35T>A
ENST00000553106.5:c.352+35T>A ENSP00000448059.1:n.352+35T>A
NM_000277.1:c.352+35T>A NP_000268.1:n.352+35T>A
XM_011538422.1:c.352+35T>A XP_011536724.1:n.352+35T>A
NM_000277.2:c.352+35T>A NP_000268.1:n.352+35T>A
NM_001354304.1:c.352+35T>A NP_001341233.1:n.352+35T>A
XM_017019370.2:c.352+35T>A XP_016874859.1:n.352+35T>A
NM_000277.3:c.352+35T>A MANE Select NP_000268.1:n.352+35T>A
NM_001354304.2:c.352+35T>A NP_001341233.1:n.352+35T>A
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