Canonical Allele Identifier: CA229395
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102565
dbSNP Id: rs62507261

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102840523C>T , CM000674.2:g.102840523C>T GRCh38
NC_000012.11:g.103234301C>T , CM000674.1:g.103234301C>T GRCh37
NC_000012.10:g.101758431C>T NCBI36
NG_008690.1:g.82080G>A
NG_008690.2:g.122888G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.1200-8G>A MANE Select ENSP00000448059.1:n.1200-8G>A
ENST00000307000.7:c.1185-8G>A ENSP00000303500.2:n.1185-8G>A
ENST00000549247.6:n.959-8G>A
ENST00000551114.2:n.862-8G>A
ENST00000553106.5:c.1200-8G>A ENSP00000448059.1:n.1200-8G>A
ENST00000635477.1:c.304-8G>A
ENST00000635528.1:n.715-8G>A
NM_000277.1:c.1200-8G>A NP_000268.1:n.1200-8G>A
XM_011538422.1:c.1143-8G>A XP_011536724.1:n.1143-8G>A
NM_000277.2:c.1200-8G>A NP_000268.1:n.1200-8G>A
NM_001354304.1:c.1200-8G>A NP_001341233.1:n.1200-8G>A
NM_000277.3:c.1200-8G>A MANE Select NP_000268.1:n.1200-8G>A
NM_001354304.2:c.1200-8G>A NP_001341233.1:n.1200-8G>A