Canonical Allele Identifier: CA607148727
Gene: PAH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102916909_102916910insGCCGGGCGCGGTGGCTCACGCCTGT , CM000674.2:g.102916909_102916910insGCCGGGCGCGGTGGCTCACGCCTGT GRCh38
NC_000012.11:g.103310687_103310688insGCCGGGCGCGGTGGCTCACGCCTGT , CM000674.1:g.103310687_103310688insGCCGGGCGCGGTGGCTCACGCCTGT GRCh37
NC_000012.10:g.101834817_101834818insGCCGGGCGCGGTGGCTCACGCCTGT NCBI36
NG_008690.1:g.5693_5694insACAGGCGTGAGCCACCGCGCCCGGC
NG_008690.2:g.46501_46502insACAGGCGTGAGCCACCGCGCCCGGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.60+161_60+162insACAGGCGTGAGCCACCGCGCCCGGC MANE Select ENSP00000448059.1:n.60+161_60+162insACAGGCGTGAGCCACCGCGCCCGGC...
ENST00000307000.7:c.-88+161_-88+162insACAGGCGTGAGCCACCGCGCCCGGC ENSP00000303500.2:n.-88+161_-88+162insACAGGCGTGAGCCACCGCGCCCG...
ENST00000546844.1:c.60+161_60+162insACAGGCGTGAGCCACCGCGCCCGGC ENSP00000446658.1:n.60+161_60+162insACAGGCGTGAGCCACCGCGCCCGGC...
ENST00000547319.1:n.371+161_371+162insACAGGCGTGAGCCACCGCGCCCGGC
ENST00000549111.5:n.156+161_156+162insACAGGCGTGAGCCACCGCGCCCGGC
ENST00000550978.6:c.44+161_44+162insACAGGCGTGAGCCACCGCGCCCGGC
ENST00000551337.5:c.60+161_60+162insACAGGCGTGAGCCACCGCGCCCGGC ENSP00000447620.1:n.60+161_60+162insACAGGCGTGAGCCACCGCGCCCGGC...
ENST00000551988.5:n.149+161_149+162insACAGGCGTGAGCCACCGCGCCCGGC
ENST00000553106.5:c.60+161_60+162insACAGGCGTGAGCCACCGCGCCCGGC ENSP00000448059.1:n.60+161_60+162insACAGGCGTGAGCCACCGCGCCCGGC...
ENST00000635500.1:n.29-4012_29-4011insACAGGCGTGAGCCACCGCGCCCGGC
NM_000277.1:c.60+161_60+162insACAGGCGTGAGCCACCGCGCCCGGC NP_000268.1:n.60+161_60+162insACAGGCGTGAGCCACCGCGCCCGGC
XM_011538422.1:c.60+161_60+162insACAGGCGTGAGCCACCGCGCCCGGC XP_011536724.1:n.60+161_60+162insACAGGCGTGAGCCACCGCGCCCGGC
NM_000277.2:c.60+161_60+162insACAGGCGTGAGCCACCGCGCCCGGC NP_000268.1:n.60+161_60+162insACAGGCGTGAGCCACCGCGCCCGGC
NM_001354304.1:c.60+161_60+162insACAGGCGTGAGCCACCGCGCCCGGC NP_001341233.1:n.60+161_60+162insACAGGCGTGAGCCACCGCGCCCGGC
XM_017019370.2:c.60+161_60+162insACAGGCGTGAGCCACCGCGCCCGGC XP_016874859.1:n.60+161_60+162insACAGGCGTGAGCCACCGCGCCCGGC
NM_000277.3:c.60+161_60+162insACAGGCGTGAGCCACCGCGCCCGGC MANE Select NP_000268.1:n.60+161_60+162insACAGGCGTGAGCCACCGCGCCCGGC
NM_001354304.2:c.60+161_60+162insACAGGCGTGAGCCACCGCGCCCGGC NP_001341233.1:n.60+161_60+162insACAGGCGTGAGCCACCGCGCCCGGC