Canonical Allele Identifier: CA229398
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102567
ClinVar RCV Id: RCV000088801 RCV000758128
dbSNP Id: rs62644469
MyVariant Identifiers: chr12:g.103234276A>G (hg19) chr12:g.102840498A>G (hg38)
ERepo: CA229398/MONDO:0009861/006
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102840498A>G , CM000674.2:g.102840498A>G GRCh38
NC_000012.11:g.103234276A>G , CM000674.1:g.103234276A>G GRCh37
NC_000012.10:g.101758406A>G NCBI36
NG_008690.1:g.82105T>C
NG_008690.2:g.122913T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.1217T>C MANE Select ENSP00000448059.1:p.Ile406Thr
ENST00000307000.7:c.1202T>C ENSP00000303500.2:p.Ile401Thr
ENST00000551114.2:n.879T>C
ENST00000553106.5:c.1217T>C ENSP00000448059.1:p.Ile406Thr
ENST00000635477.1:c.321T>C
ENST00000635528.1:n.732T>C
NM_000277.1:c.1217T>C NP_000268.1:p.Ile406Thr
XM_011538422.1:c.1160T>C XP_011536724.1:p.Ile387Thr
NM_000277.2:c.1217T>C NP_000268.1:p.Ile406Thr
NM_001354304.1:c.1217T>C NP_001341233.1:p.Ile406Thr
NM_000277.3:c.1217T>C MANE Select NP_000268.1:p.Ile406Thr
NM_001354304.2:c.1217T>C NP_001341233.1:p.Ile406Thr
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