Canonical Allele Identifier: CA229857

Gene: PAH

Linked Data

• ClinVar Variation Id: 102901
• ClinVar RCV Id: RCV000089165 ; RCV001269049
• dbSNP Id: rs62642915
• MyVariant Identifiers: chr12:g.103240707C>T (hg19) ; chr12:g.102846929C>T (hg38)
• ERepo: CA229857/MONDO:0009861/006

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.102846929C>T , CM000674.2:g.102846929C>T	GRCh38
NC_000012.11:g.103240707C>T , CM000674.1:g.103240707C>T	GRCh37
NC_000012.10:g.101764837C>T	NCBI36
NG_008690.1:g.75674G>A
NG_008690.2:g.116482G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553106.6:c.935G>A MANE Select	ENSP00000448059.1:p.Gly312Asp
ENST00000307000.7:c.920G>A	ENSP00000303500.2:p.Gly307Asp
ENST00000549247.6:n.694G>A
ENST00000551114.2:n.597G>A
ENST00000553106.5:c.935G>A	ENSP00000448059.1:p.Gly312Asp
ENST00000635477.1:c.74-2498G>A
ENST00000635528.1:n.450G>A
NM_000277.1:c.935G>A	NP_000268.1:p.Gly312Asp
XM_011538422.1:c.913-2498G>A	XP_011536724.1:n.913-2498G>A
NM_000277.2:c.935G>A	NP_000268.1:p.Gly312Asp
NM_001354304.1:c.935G>A	NP_001341233.1:p.Gly312Asp
NM_000277.3:c.935G>A MANE Select	NP_000268.1:p.Gly312Asp
NM_001354304.2:c.935G>A	NP_001341233.1:p.Gly312Asp