Canonical Allele Identifier: CA386493113
Gene: PAH HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.103234291T>G (hg19) chr12:g.102840513T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102840513T>G , CM000674.2:g.102840513T>G GRCh38
NC_000012.11:g.103234291T>G , CM000674.1:g.103234291T>G GRCh37
NC_000012.10:g.101758421T>G NCBI36
NG_008690.1:g.82090A>C
NG_008690.2:g.122898A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.1202A>C MANE Select ENSP00000448059.1:p.Asn401Thr
ENST00000307000.7:c.1187A>C ENSP00000303500.2:p.Asn396Thr
ENST00000549247.6:n.961A>C
ENST00000551114.2:n.864A>C
ENST00000553106.5:c.1202A>C ENSP00000448059.1:p.Asn401Thr
ENST00000635477.1:c.306A>C
ENST00000635528.1:n.717A>C
NM_000277.1:c.1202A>C NP_000268.1:p.Asn401Thr
XM_011538422.1:c.1145A>C XP_011536724.1:p.Asn382Thr
NM_000277.2:c.1202A>C NP_000268.1:p.Asn401Thr
NM_001354304.1:c.1202A>C NP_001341233.1:p.Asn401Thr
NM_000277.3:c.1202A>C MANE Select NP_000268.1:p.Asn401Thr
NM_001354304.2:c.1202A>C NP_001341233.1:p.Asn401Thr
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