Canonical Allele Identifier: CA229516

Gene: PAH

Linked Data

• ClinVar Variation Id: 102651
• ClinVar RCV Id: RCV000088897 ; RCV002259587
• dbSNP Id: rs199475627
• MyVariant Identifiers: chr12:g.103288536G>A (hg19) ; chr12:g.102894758G>A (hg38)
• ERepo: CA229516/MONDO:0009861/006

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.102894758G>A , CM000674.2:g.102894758G>A	GRCh38
NC_000012.11:g.103288536G>A , CM000674.1:g.103288536G>A	GRCh37
NC_000012.10:g.101812666G>A	NCBI36
NG_008690.1:g.27845C>T
NG_008690.2:g.68653C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553106.6:c.329C>T MANE Select	ENSP00000448059.1:p.Ser110Leu
ENST00000307000.7:c.314C>T	ENSP00000303500.2:p.Ser105Leu
ENST00000546844.1:c.329C>T	ENSP00000446658.1:p.Ser110Leu
ENST00000548928.1:n.251C>T
ENST00000549111.5:n.425C>T
ENST00000550978.6:c.313C>T
ENST00000551337.5:c.329C>T	ENSP00000447620.1:p.Ser110Leu
ENST00000551988.5:n.418C>T
ENST00000553106.5:c.329C>T	ENSP00000448059.1:p.Ser110Leu
NM_000277.1:c.329C>T	NP_000268.1:p.Ser110Leu
XM_011538422.1:c.329C>T	XP_011536724.1:p.Ser110Leu
NM_000277.2:c.329C>T	NP_000268.1:p.Ser110Leu
NM_001354304.1:c.329C>T	NP_001341233.1:p.Ser110Leu
XM_017019370.2:c.329C>T	XP_016874859.1:p.Ser110Leu
NM_000277.3:c.329C>T MANE Select	NP_000268.1:p.Ser110Leu
NM_001354304.2:c.329C>T	NP_001341233.1:p.Ser110Leu