Canonical Allele Identifier: CA229480

Gene: PAH

Linked Data

• ClinVar Variation Id: 102624
• ClinVar RCV Id: RCV000088866
• dbSNP Id: rs75193786
• MyVariant Identifiers: chr12:g.103288671A>C (hg19) ; chr12:g.102894893A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.102894893A>C , CM000674.2:g.102894893A>C	GRCh38
NC_000012.11:g.103288671A>C , CM000674.1:g.103288671A>C	GRCh37
NC_000012.10:g.101812801A>C	NCBI36
NG_008690.1:g.27710T>G
NG_008690.2:g.68518T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553106.6:c.194T>G MANE Select	ENSP00000448059.1:p.Ile65Ser
ENST00000307000.7:c.179T>G	ENSP00000303500.2:p.Ile60Ser
ENST00000546844.1:c.194T>G	ENSP00000446658.1:p.Ile65Ser
ENST00000548677.2:n.281T>G
ENST00000548928.1:n.116T>G
ENST00000549111.5:n.290T>G
ENST00000550978.6:c.178T>G
ENST00000551337.5:c.194T>G	ENSP00000447620.1:p.Ile65Ser
ENST00000551988.5:n.283T>G
ENST00000553106.5:c.194T>G	ENSP00000448059.1:p.Ile65Ser
ENST00000635500.1:n.162T>G
NM_000277.1:c.194T>G	NP_000268.1:p.Ile65Ser
XM_011538422.1:c.194T>G	XP_011536724.1:p.Ile65Ser
NM_000277.2:c.194T>G	NP_000268.1:p.Ile65Ser
NM_001354304.1:c.194T>G	NP_001341233.1:p.Ile65Ser
XM_017019370.2:c.194T>G	XP_016874859.1:p.Ile65Ser
NM_000277.3:c.194T>G MANE Select	NP_000268.1:p.Ile65Ser
NM_001354304.2:c.194T>G	NP_001341233.1:p.Ile65Ser