Canonical Allele Identifier: CA386303960

Gene: PAH

Linked Data

• MyVariant Identifiers: chr12:g.103288530T>A (hg19) ; chr12:g.102894752T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.102894752T>A , CM000674.2:g.102894752T>A	GRCh38
NC_000012.11:g.103288530T>A , CM000674.1:g.103288530T>A	GRCh37
NC_000012.10:g.101812660T>A	NCBI36
NG_008690.1:g.27851A>T
NG_008690.2:g.68659A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553106.6:c.335A>T MANE Select	ENSP00000448059.1:p.Asp112Val
ENST00000307000.7:c.320A>T	ENSP00000303500.2:p.Asp107Val
ENST00000546844.1:c.335A>T	ENSP00000446658.1:p.Asp112Val
ENST00000548928.1:n.257A>T
ENST00000549111.5:n.431A>T
ENST00000550978.6:c.319A>T
ENST00000551337.5:c.335A>T	ENSP00000447620.1:p.Asp112Val
ENST00000551988.5:n.424A>T
ENST00000553106.5:c.335A>T	ENSP00000448059.1:p.Asp112Val
NM_000277.1:c.335A>T	NP_000268.1:p.Asp112Val
XM_011538422.1:c.335A>T	XP_011536724.1:p.Asp112Val
NM_000277.2:c.335A>T	NP_000268.1:p.Asp112Val
NM_001354304.1:c.335A>T	NP_001341233.1:p.Asp112Val
XM_017019370.2:c.335A>T	XP_016874859.1:p.Asp112Val
NM_000277.3:c.335A>T MANE Select	NP_000268.1:p.Asp112Val
NM_001354304.2:c.335A>T	NP_001341233.1:p.Asp112Val