Canonical Allele Identifier: CA16020921

Gene: PAH

Linked Data

• ClinVar Variation Id: 458078
• ClinVar RCV Id: RCV000553622
• dbSNP Id: rs1555203737
• MyVariant Identifiers: chr12:g.103238142C>T (hg19) ; chr12:g.102844364C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.102844364C>T , CM000674.2:g.102844364C>T	GRCh38
NC_000012.11:g.103238142C>T , CM000674.1:g.103238142C>T	GRCh37
NC_000012.10:g.101762272C>T	NCBI36
NG_008690.1:g.78239G>A
NG_008690.2:g.119047G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553106.6:c.1037G>A MANE Select	ENSP00000448059.1:p.Gly346Glu
ENST00000307000.7:c.1022G>A	ENSP00000303500.2:p.Gly341Glu
ENST00000549247.6:n.796G>A
ENST00000551114.2:n.699G>A
ENST00000553106.5:c.1037G>A	ENSP00000448059.1:p.Gly346Glu
ENST00000635477.1:c.141G>A
ENST00000635528.1:n.552G>A
NM_000277.1:c.1037G>A	NP_000268.1:p.Gly346Glu
XM_011538422.1:c.980G>A	XP_011536724.1:p.Gly327Glu
NM_000277.2:c.1037G>A	NP_000268.1:p.Gly346Glu
NM_001354304.1:c.1037G>A	NP_001341233.1:p.Gly346Glu
NM_000277.3:c.1037G>A MANE Select	NP_000268.1:p.Gly346Glu
NM_001354304.2:c.1037G>A	NP_001341233.1:p.Gly346Glu