Canonical Allele Identifier: CA275935

Gene: PAH

Linked Data

• ClinVar Variation Id: 208179
• ClinVar RCV Id: RCV000190375
• dbSNP Id: rs796064501
• MyVariant Identifiers: chr12:g.103238154G>T (hg19) ; chr12:g.102844376G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.102844376G>T , CM000674.2:g.102844376G>T	GRCh38
NC_000012.11:g.103238154G>T , CM000674.1:g.103238154G>T	GRCh37
NC_000012.10:g.101762284G>T	NCBI36
NG_008690.1:g.78227C>A
NG_008690.2:g.119035C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553106.6:c.1025C>A MANE Select	ENSP00000448059.1:p.Ala342Glu
ENST00000307000.7:c.1010C>A	ENSP00000303500.2:p.Ala337Glu
ENST00000549247.6:n.784C>A
ENST00000551114.2:n.687C>A
ENST00000553106.5:c.1025C>A	ENSP00000448059.1:p.Ala342Glu
ENST00000635477.1:c.129C>A
ENST00000635528.1:n.540C>A
NM_000277.1:c.1025C>A	NP_000268.1:p.Ala342Glu
XM_011538422.1:c.968C>A	XP_011536724.1:p.Ala323Glu
NM_000277.2:c.1025C>A	NP_000268.1:p.Ala342Glu
NM_001354304.1:c.1025C>A	NP_001341233.1:p.Ala342Glu
NM_000277.3:c.1025C>A MANE Select	NP_000268.1:p.Ala342Glu
NM_001354304.2:c.1025C>A	NP_001341233.1:p.Ala342Glu