Canonical Allele Identifier: CA386302629

Gene: PAH

Linked Data

• MyVariant Identifiers: chr12:g.103306645T>C (hg19) ; chr12:g.102912867T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.102912867T>C , CM000674.2:g.102912867T>C	GRCh38
NC_000012.11:g.103306645T>C , CM000674.1:g.103306645T>C	GRCh37
NC_000012.10:g.101830775T>C	NCBI36
NG_008690.1:g.9736A>G
NG_008690.2:g.50544A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553106.6:c.92A>G MANE Select	ENSP00000448059.1:p.Gln31Arg
ENST00000307000.7:c.77A>G	ENSP00000303500.2:p.Gln26Arg
ENST00000546844.1:c.92A>G	ENSP00000446658.1:p.Gln31Arg
ENST00000548677.2:n.179A>G
ENST00000548928.1:n.14A>G
ENST00000549111.5:n.188A>G
ENST00000550978.6:c.76A>G
ENST00000551337.5:c.92A>G	ENSP00000447620.1:p.Gln31Arg
ENST00000551988.5:n.181A>G
ENST00000553106.5:c.92A>G	ENSP00000448059.1:p.Gln31Arg
ENST00000635500.1:n.60A>G
NM_000277.1:c.92A>G	NP_000268.1:p.Gln31Arg
XM_011538422.1:c.92A>G	XP_011536724.1:p.Gln31Arg
NM_000277.2:c.92A>G	NP_000268.1:p.Gln31Arg
NM_001354304.1:c.92A>G	NP_001341233.1:p.Gln31Arg
XM_017019370.2:c.92A>G	XP_016874859.1:p.Gln31Arg
NM_000277.3:c.92A>G MANE Select	NP_000268.1:p.Gln31Arg
NM_001354304.2:c.92A>G	NP_001341233.1:p.Gln31Arg