Canonical Allele Identifier: CA386303796
Gene: PAH HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.103310853C>A (hg19) chr12:g.102917075C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102917075C>A , CM000674.2:g.102917075C>A GRCh38
NC_000012.11:g.103310853C>A , CM000674.1:g.103310853C>A GRCh37
NC_000012.10:g.101834983C>A NCBI36
NG_008690.1:g.5528G>T
NG_008690.2:g.46336G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.56G>T MANE Select ENSP00000448059.1:p.Gly19Val
ENST00000307000.7:c.-92G>T ENSP00000303500.2:n.-92G>T
ENST00000546844.1:c.56G>T ENSP00000446658.1:p.Gly19Val
ENST00000547319.1:n.367G>T
ENST00000549111.5:n.152G>T
ENST00000550978.6:c.40G>T
ENST00000551337.5:c.56G>T ENSP00000447620.1:p.Gly19Val
ENST00000551988.5:n.145G>T
ENST00000553106.5:c.56G>T ENSP00000448059.1:p.Gly19Val
ENST00000635500.1:n.29-4177G>T
NM_000277.1:c.56G>T NP_000268.1:p.Gly19Val
XM_011538422.1:c.56G>T XP_011536724.1:p.Gly19Val
NM_000277.2:c.56G>T NP_000268.1:p.Gly19Val
NM_001354304.1:c.56G>T NP_001341233.1:p.Gly19Val
XM_017019370.2:c.56G>T XP_016874859.1:p.Gly19Val
NM_000277.3:c.56G>T MANE Select NP_000268.1:p.Gly19Val
NM_001354304.2:c.56G>T NP_001341233.1:p.Gly19Val
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