Canonical Allele Identifier: CA386493298
Gene: PAH HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.103237518G>T (hg19) chr12:g.102843740G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102843740G>T , CM000674.2:g.102843740G>T GRCh38
NC_000012.11:g.103237518G>T , CM000674.1:g.103237518G>T GRCh37
NC_000012.10:g.101761648G>T NCBI36
NG_008690.1:g.78863C>A
NG_008690.2:g.119671C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.1105C>A MANE Select ENSP00000448059.1:p.Leu369Met
ENST00000307000.7:c.1090C>A ENSP00000303500.2:p.Leu364Met
ENST00000549247.6:n.864C>A
ENST00000551114.2:n.767C>A
ENST00000553106.5:c.1105C>A ENSP00000448059.1:p.Leu369Met
ENST00000635477.1:c.209C>A
ENST00000635528.1:n.620C>A
NM_000277.1:c.1105C>A NP_000268.1:p.Leu369Met
XM_011538422.1:c.1048C>A XP_011536724.1:p.Leu350Met
NM_000277.2:c.1105C>A NP_000268.1:p.Leu369Met
NM_001354304.1:c.1105C>A NP_001341233.1:p.Leu369Met
NM_000277.3:c.1105C>A MANE Select NP_000268.1:p.Leu369Met
NM_001354304.2:c.1105C>A NP_001341233.1:p.Leu369Met
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