Canonical Allele Identifier: CA2059446897

Gene: PAH

Linked Data

• dbSNP Id: rs1381169797

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.102853047C>G , CM000674.2:g.102853047C>G	GRCh38
NC_000012.11:g.103246825C>G , CM000674.1:g.103246825C>G	GRCh37
NC_000012.10:g.101770955C>G	NCBI36
NG_008690.1:g.69556G>C
NG_008690.2:g.110364G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553106.6:c.707-97G>C MANE Select	ENSP00000448059.1:n.707-97G>C
ENST00000307000.7:c.692-97G>C	ENSP00000303500.2:n.692-97G>C
ENST00000549247.6:n.369G>C
ENST00000553106.5:c.707-97G>C	ENSP00000448059.1:n.707-97G>C
NM_000277.1:c.707-97G>C	NP_000268.1:n.707-97G>C
XM_011538422.1:c.707-97G>C	XP_011536724.1:n.707-97G>C
NM_000277.2:c.707-97G>C	NP_000268.1:n.707-97G>C
NM_001354304.1:c.707-97G>C	NP_001341233.1:n.707-97G>C
NM_000277.3:c.707-97G>C MANE Select	NP_000268.1:n.707-97G>C
NM_001354304.2:c.707-97G>C	NP_001341233.1:n.707-97G>C