Canonical Allele Identifier: CA655298587
Gene: PAH HGNC NCBI

Linked Data

COSMIC: COSN2374835
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102917136C>T , CM000674.2:g.102917136C>T GRCh38
NC_000012.11:g.103310914C>T , CM000674.1:g.103310914C>T GRCh37
NC_000012.10:g.101835044C>T NCBI36
NG_008690.1:g.5467G>A
NG_008690.2:g.46275G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.-6G>A MANE Select ENSP00000448059.1:n.-6G>A
ENST00000307000.7:c.-153G>A ENSP00000303500.2:n.-153G>A
ENST00000546844.1:c.-6G>A ENSP00000446658.1:n.-6G>A
ENST00000547319.1:n.306G>A
ENST00000549111.5:n.91G>A
ENST00000551337.5:c.-6G>A ENSP00000447620.1:n.-6G>A
ENST00000551988.5:n.84G>A
ENST00000553106.5:c.-6G>A ENSP00000448059.1:n.-6G>A
ENST00000635500.1:n.29-4238G>A
NM_000277.1:c.-6G>A NP_000268.1:n.-6G>A
XM_011538422.1:c.-6G>A XP_011536724.1:n.-6G>A
NM_000277.2:c.-6G>A NP_000268.1:n.-6G>A
NM_001354304.1:c.-6G>A NP_001341233.1:n.-6G>A
XM_017019370.2:c.-6G>A XP_016874859.1:n.-6G>A
NM_000277.3:c.-6G>A MANE Select NP_000268.1:n.-6G>A
NM_001354304.2:c.-6G>A NP_001341233.1:n.-6G>A
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