Canonical Allele Identifier: CA386295593
Gene: PAH HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.103246670C>G (hg19) chr12:g.102852892C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102852892C>G , CM000674.2:g.102852892C>G GRCh38
NC_000012.11:g.103246670C>G , CM000674.1:g.103246670C>G GRCh37
NC_000012.10:g.101770800C>G NCBI36
NG_008690.1:g.69711G>C
NG_008690.2:g.110519G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.765G>C MANE Select ENSP00000448059.1:p.Leu255Phe
ENST00000307000.7:c.750G>C ENSP00000303500.2:p.Leu250Phe
ENST00000549247.6:n.524G>C
ENST00000553106.5:c.765G>C ENSP00000448059.1:p.Leu255Phe
NM_000277.1:c.765G>C NP_000268.1:p.Leu255Phe
XM_011538422.1:c.765G>C XP_011536724.1:p.Leu255Phe
NM_000277.2:c.765G>C NP_000268.1:p.Leu255Phe
NM_001354304.1:c.765G>C NP_001341233.1:p.Leu255Phe
NM_000277.3:c.765G>C MANE Select NP_000268.1:p.Leu255Phe
NM_001354304.2:c.765G>C NP_001341233.1:p.Leu255Phe
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