Canonical Allele Identifier: CA2739277293
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 2806388
ClinVar RCV Id: RCV003598929
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102855125T>G , CM000674.2:g.102855125T>G GRCh38
NC_000012.11:g.103248903T>G , CM000674.1:g.103248903T>G GRCh37
NC_000012.10:g.101773033T>G NCBI36
NG_008690.1:g.67478A>C
NG_008690.2:g.108286A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.706+11A>C MANE Select ENSP00000448059.1:n.706+11A>C
ENST00000307000.7:c.691+11A>C ENSP00000303500.2:n.691+11A>C
ENST00000549111.5:n.813A>C
ENST00000553106.5:c.706+11A>C ENSP00000448059.1:n.706+11A>C
NM_000277.1:c.706+11A>C NP_000268.1:n.706+11A>C
XM_011538422.1:c.706+11A>C XP_011536724.1:n.706+11A>C
NM_000277.2:c.706+11A>C NP_000268.1:n.706+11A>C
NM_001354304.1:c.706+11A>C NP_001341233.1:n.706+11A>C
XM_017019370.2:c.706+11A>C XP_016874859.1:n.706+11A>C
NM_000277.3:c.706+11A>C MANE Select NP_000268.1:n.706+11A>C
NM_001354304.2:c.706+11A>C NP_001341233.1:n.706+11A>C
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