Canonical Allele Identifier: CA2620508998
Gene: PAH HGNC NCBI

Linked Data

gnomAD v4: 12-102846745-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102846745T>A , CM000674.2:g.102846745T>A GRCh38
NC_000012.11:g.103240523T>A , CM000674.1:g.103240523T>A GRCh37
NC_000012.10:g.101764653T>A NCBI36
NG_008690.1:g.75858A>T
NG_008690.2:g.116666A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.969+150A>T MANE Select ENSP00000448059.1:n.969+150A>T
ENST00000307000.7:c.954+150A>T ENSP00000303500.2:n.954+150A>T
ENST00000549247.6:n.728+150A>T
ENST00000551114.2:n.631+150A>T
ENST00000553106.5:c.969+150A>T ENSP00000448059.1:n.969+150A>T
ENST00000635477.1:c.74-2314A>T
ENST00000635528.1:n.484+150A>T
NM_000277.1:c.969+150A>T NP_000268.1:n.969+150A>T
XM_011538422.1:c.913-2314A>T XP_011536724.1:n.913-2314A>T
NM_000277.2:c.969+150A>T NP_000268.1:n.969+150A>T
NM_001354304.1:c.969+150A>T NP_001341233.1:n.969+150A>T
NM_000277.3:c.969+150A>T MANE Select NP_000268.1:n.969+150A>T
NM_001354304.2:c.969+150A>T NP_001341233.1:n.969+150A>T
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