Canonical Allele Identifier: CA951244235
Gene: PAH HGNC NCBI

Linked Data

gnomAD v3: 12-102894429-T-TAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAATAAAAAATAAAAAATTAAAAAAAA
gnomAD v4: 12-102894429-T-TAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAATAAAAAATAAAAAATTAAAAAAAA
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102894441_102894442insAAAAAAAAAAAAAAAAAAAAAATAAAAAATAAAAAATTAAAAAAAAAAAAAAAAAAAA , CM000674.2:g.102894441_102894442insAAAAAAAAAAAAAAAAAAAAAATAAAAAATAAAAAATTAAAAAAAAAAAAAAAAAAAA GRCh38
NC_000012.11:g.103288219_103288220insAAAAAAAAAAAAAAAAAAAAAATAAAAAATAAAAAATTAAAAAAAAAAAAAAAAAAAA , CM000674.1:g.103288219_103288220insAAAAAAAAAAAAAAAAAAAAAATAAAAAATAAAAAATTAAAAAAAAAAAAAAAAAAAA GRCh37
NC_000012.10:g.101812349_101812350insAAAAAAAAAAAAAAAAAAAAAATAAAAAATAAAAAATTAAAAAAAAAAAAAAAAAAAA NCBI36
NG_008690.1:g.28173_28174insTTTTTTTTAATTTTTTATTTTTTATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
NG_008690.2:g.68981_68982insTTTTTTTTAATTTTTTATTTTTTATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.352+305_352+306insTTTTTTTTAATTTTTTATTTTTTATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT MANE Select ENSP00000448059.1:n.352+305_352+306insTTTTTTTTAATTTTTTATTTTTT...
ENST00000307000.7:c.337+305_337+306insTTTTTTTTAATTTTTTATTTTTTATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT ENSP00000303500.2:n.337+305_337+306insTTTTTTTTAATTTTTTATTTTTT...
ENST00000548928.1:n.274+305_274+306insTTTTTTTTAATTTTTTATTTTTTATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
ENST00000549111.5:n.448+305_448+306insTTTTTTTTAATTTTTTATTTTTTATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
ENST00000550978.6:c.336+305_336+306insTTTTTTTTAATTTTTTATTTTTTATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
ENST00000551337.5:c.352+305_352+306insTTTTTTTTAATTTTTTATTTTTTATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT ENSP00000447620.1:n.352+305_352+306insTTTTTTTTAATTTTTTATTTTTT...
ENST00000551988.5:n.441+305_441+306insTTTTTTTTAATTTTTTATTTTTTATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
ENST00000553106.5:c.352+305_352+306insTTTTTTTTAATTTTTTATTTTTTATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT ENSP00000448059.1:n.352+305_352+306insTTTTTTTTAATTTTTTATTTTTT...
NM_000277.1:c.352+305_352+306insTTTTTTTTAATTTTTTATTTTTTATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT NP_000268.1:n.352+305_352+306insTTTTTTTTAATTTTTTATTTTTTATTTTT...
XM_011538422.1:c.352+305_352+306insTTTTTTTTAATTTTTTATTTTTTATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT XP_011536724.1:n.352+305_352+306insTTTTTTTTAATTTTTTATTTTTTATT...
NM_000277.2:c.352+305_352+306insTTTTTTTTAATTTTTTATTTTTTATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT NP_000268.1:n.352+305_352+306insTTTTTTTTAATTTTTTATTTTTTATTTTT...
NM_001354304.1:c.352+305_352+306insTTTTTTTTAATTTTTTATTTTTTATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT NP_001341233.1:n.352+305_352+306insTTTTTTTTAATTTTTTATTTTTTATT...
XM_017019370.2:c.352+305_352+306insTTTTTTTTAATTTTTTATTTTTTATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT XP_016874859.1:n.352+305_352+306insTTTTTTTTAATTTTTTATTTTTTATT...
NM_000277.3:c.352+305_352+306insTTTTTTTTAATTTTTTATTTTTTATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT MANE Select NP_000268.1:n.352+305_352+306insTTTTTTTTAATTTTTTATTTTTTATTTTT...
NM_001354304.2:c.352+305_352+306insTTTTTTTTAATTTTTTATTTTTTATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT NP_001341233.1:n.352+305_352+306insTTTTTTTTAATTTTTTATTTTTTATT...
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