Canonical Allele Identifier: CA386303925

Gene: PAH

Linked Data

• MyVariant Identifiers: chr12:g.103288516T>A (hg19) ; chr12:g.102894738T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.102894738T>A , CM000674.2:g.102894738T>A	GRCh38
NC_000012.11:g.103288516T>A , CM000674.1:g.103288516T>A	GRCh37
NC_000012.10:g.101812646T>A	NCBI36
NG_008690.1:g.27865A>T
NG_008690.2:g.68673A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000553106.6:c.349A>T MANE Select	ENSP00000448059.1:p.Thr117Ser
ENST00000307000.7:c.334A>T	ENSP00000303500.2:p.Thr112Ser
ENST00000546844.1:c.349A>T	ENSP00000446658.1:p.Thr117Ser
ENST00000548928.1:n.271A>T
ENST00000549111.5:n.445A>T
ENST00000550978.6:c.333A>T
ENST00000551337.5:c.349A>T	ENSP00000447620.1:p.Thr117Ser
ENST00000551988.5:n.438A>T
ENST00000553106.5:c.349A>T	ENSP00000448059.1:p.Thr117Ser
NM_000277.1:c.349A>T	NP_000268.1:p.Thr117Ser
XM_011538422.1:c.349A>T	XP_011536724.1:p.Thr117Ser
NM_000277.2:c.349A>T	NP_000268.1:p.Thr117Ser
NM_001354304.1:c.349A>T	NP_001341233.1:p.Thr117Ser
XM_017019370.2:c.349A>T	XP_016874859.1:p.Thr117Ser
NM_000277.3:c.349A>T MANE Select	NP_000268.1:p.Thr117Ser
NM_001354304.2:c.349A>T	NP_001341233.1:p.Thr117Ser