Canonical Allele Identifier: CA386302278

Gene: PAH

Linked Data

• MyVariant Identifiers: chr12:g.103306570T>A (hg19) ; chr12:g.102912792T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.102912792T>A , CM000674.2:g.102912792T>A	GRCh38
NC_000012.11:g.103306570T>A , CM000674.1:g.103306570T>A	GRCh37
NC_000012.10:g.101830700T>A	NCBI36
NG_008690.1:g.9811A>T
NG_008690.2:g.50619A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000553106.6:c.167A>T MANE Select	ENSP00000448059.1:p.Glu56Val
ENST00000307000.7:c.152A>T	ENSP00000303500.2:p.Glu51Val
ENST00000546844.1:c.167A>T	ENSP00000446658.1:p.Glu56Val
ENST00000548677.2:n.254A>T
ENST00000548928.1:n.89A>T
ENST00000549111.5:n.263A>T
ENST00000550978.6:c.151A>T
ENST00000551337.5:c.167A>T	ENSP00000447620.1:p.Glu56Val
ENST00000551988.5:n.256A>T
ENST00000553106.5:c.167A>T	ENSP00000448059.1:p.Glu56Val
ENST00000635500.1:n.135A>T
NM_000277.1:c.167A>T	NP_000268.1:p.Glu56Val
XM_011538422.1:c.167A>T	XP_011536724.1:p.Glu56Val
NM_000277.2:c.167A>T	NP_000268.1:p.Glu56Val
NM_001354304.1:c.167A>T	NP_001341233.1:p.Glu56Val
XM_017019370.2:c.167A>T	XP_016874859.1:p.Glu56Val
NM_000277.3:c.167A>T MANE Select	NP_000268.1:p.Glu56Val
NM_001354304.2:c.167A>T	NP_001341233.1:p.Glu56Val