Canonical Allele Identifier: CA16020734
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 555212
ClinVar RCV Id: RCV000670987
dbSNP Id: rs1226613045

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102894920T>C , CM000674.2:g.102894920T>C GRCh38
NC_000012.11:g.103288698T>C , CM000674.1:g.103288698T>C GRCh37
NC_000012.10:g.101812828T>C NCBI36
NG_008690.1:g.27683A>G
NG_008690.2:g.68491A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.169-2A>G MANE Select ENSP00000448059.1:n.169-2A>G
ENST00000307000.7:c.154-2A>G ENSP00000303500.2:n.154-2A>G
ENST00000546844.1:c.169-2A>G ENSP00000446658.1:n.169-2A>G
ENST00000548677.2:n.256-2A>G
ENST00000548928.1:n.91-2A>G
ENST00000549111.5:n.265-2A>G
ENST00000550978.6:c.153-2A>G
ENST00000551337.5:c.169-2A>G ENSP00000447620.1:n.169-2A>G
ENST00000551988.5:n.258-2A>G
ENST00000553106.5:c.169-2A>G ENSP00000448059.1:n.169-2A>G
ENST00000635500.1:n.137-2A>G
NM_000277.1:c.169-2A>G NP_000268.1:n.169-2A>G
XM_011538422.1:c.169-2A>G XP_011536724.1:n.169-2A>G
NM_000277.2:c.169-2A>G NP_000268.1:n.169-2A>G
NM_001354304.1:c.169-2A>G NP_001341233.1:n.169-2A>G
XM_017019370.2:c.169-2A>G XP_016874859.1:n.169-2A>G
NM_000277.3:c.169-2A>G MANE Select NP_000268.1:n.169-2A>G
NM_001354304.2:c.169-2A>G NP_001341233.1:n.169-2A>G