Canonical Allele Identifier: CA2620508183
Gene: PAH HGNC NCBI

Linked Data

gnomAD v4: 12-102913017-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102913017A>G , CM000674.2:g.102913017A>G GRCh38
NC_000012.11:g.103306795A>G , CM000674.1:g.103306795A>G GRCh37
NC_000012.10:g.101830925A>G NCBI36
NG_008690.1:g.9586T>C
NG_008690.2:g.50394T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.61-119T>C MANE Select ENSP00000448059.1:n.61-119T>C
ENST00000307000.7:c.46-119T>C ENSP00000303500.2:n.46-119T>C
ENST00000546844.1:c.61-119T>C ENSP00000446658.1:n.61-119T>C
ENST00000548677.2:n.148-119T>C
ENST00000549111.5:n.157-119T>C
ENST00000550978.6:c.45-119T>C
ENST00000551337.5:c.61-119T>C ENSP00000447620.1:n.61-119T>C
ENST00000551988.5:n.150-119T>C
ENST00000553106.5:c.61-119T>C ENSP00000448059.1:n.61-119T>C
ENST00000635500.1:n.29-119T>C
NM_000277.1:c.61-119T>C NP_000268.1:n.61-119T>C
XM_011538422.1:c.61-119T>C XP_011536724.1:n.61-119T>C
NM_000277.2:c.61-119T>C NP_000268.1:n.61-119T>C
NM_001354304.1:c.61-119T>C NP_001341233.1:n.61-119T>C
XM_017019370.2:c.61-119T>C XP_016874859.1:n.61-119T>C
NM_000277.3:c.61-119T>C MANE Select NP_000268.1:n.61-119T>C
NM_001354304.2:c.61-119T>C NP_001341233.1:n.61-119T>C
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