Canonical Allele Identifier: CA682803882

Gene: PAH

Linked Data

• dbSNP Id: rs917895089
• MyVariant Identifiers: chr12:g.103245592T>C (hg19) ; chr12:g.102851814T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.102851814T>C , CM000674.2:g.102851814T>C	GRCh38
NC_000012.11:g.103245592T>C , CM000674.1:g.103245592T>C	GRCh37
NC_000012.10:g.101769722T>C	NCBI36
NG_008690.1:g.70789A>G
NG_008690.2:g.111597A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553106.6:c.843-58A>G MANE Select	ENSP00000448059.1:n.843-58A>G
ENST00000307000.7:c.828-58A>G	ENSP00000303500.2:n.828-58A>G
ENST00000549247.6:n.602-58A>G
ENST00000551114.2:n.447A>G
ENST00000553106.5:c.843-58A>G	ENSP00000448059.1:n.843-58A>G
ENST00000635477.1:c.4-58A>G
NM_000277.1:c.843-58A>G	NP_000268.1:n.843-58A>G
XM_011538422.1:c.843-58A>G	XP_011536724.1:n.843-58A>G
NM_000277.2:c.843-58A>G	NP_000268.1:n.843-58A>G
NM_001354304.1:c.843-58A>G	NP_001341233.1:n.843-58A>G
NM_000277.3:c.843-58A>G MANE Select	NP_000268.1:n.843-58A>G
NM_001354304.2:c.843-58A>G	NP_001341233.1:n.843-58A>G