Canonical Allele Identifier: CA2059467403
Gene: PAH HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102895061_102895062delinsCT , CM000674.2:g.102895061_102895062delinsCT GRCh38
NC_000012.11:g.103288839_103288840delinsCT , CM000674.1:g.103288839_103288840delinsCT GRCh37
NC_000012.10:g.101812969_101812970delinsCT NCBI36
NG_008690.1:g.27541_27542delinsAG
NG_008690.2:g.68349_68350delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.169-144_169-143delinsAG MANE Select ENSP00000448059.1:n.169-144_169-143delinsAG
ENST00000307000.7:c.154-144_154-143delinsAG ENSP00000303500.2:n.154-144_154-143delinsAG
ENST00000546844.1:c.169-144_169-143delinsAG ENSP00000446658.1:n.169-144_169-143delinsAG
ENST00000548677.2:n.256-144_256-143delinsAG
ENST00000548928.1:n.91-144_91-143delinsAG
ENST00000549111.5:n.265-144_265-143delinsAG
ENST00000550978.6:c.153-144_153-143delinsAG
ENST00000551337.5:c.169-144_169-143delinsAG ENSP00000447620.1:n.169-144_169-143delinsAG
ENST00000551988.5:n.258-144_258-143delinsAG
ENST00000553106.5:c.169-144_169-143delinsAG ENSP00000448059.1:n.169-144_169-143delinsAG
ENST00000635500.1:n.137-144_137-143delinsAG
NM_000277.1:c.169-144_169-143delinsAG NP_000268.1:n.169-144_169-143delinsAG
XM_011538422.1:c.169-144_169-143delinsAG XP_011536724.1:n.169-144_169-143delinsAG
NM_000277.2:c.169-144_169-143delinsAG NP_000268.1:n.169-144_169-143delinsAG
NM_001354304.1:c.169-144_169-143delinsAG NP_001341233.1:n.169-144_169-143delinsAG
XM_017019370.2:c.169-144_169-143delinsAG XP_016874859.1:n.169-144_169-143delinsAG
NM_000277.3:c.169-144_169-143delinsAG MANE Select NP_000268.1:n.169-144_169-143delinsAG
NM_001354304.2:c.169-144_169-143delinsAG NP_001341233.1:n.169-144_169-143delinsAG
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