Canonical Allele Identifier: CA386493166
Gene: PAH HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.103237446T>A (hg19) chr12:g.102843668T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102843668T>A , CM000674.2:g.102843668T>A GRCh38
NC_000012.11:g.103237446T>A , CM000674.1:g.103237446T>A GRCh37
NC_000012.10:g.101761576T>A NCBI36
NG_008690.1:g.78935A>T
NG_008690.2:g.119743A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.1177A>T MANE Select ENSP00000448059.1:p.Asn393Tyr
ENST00000307000.7:c.1162A>T ENSP00000303500.2:p.Asn388Tyr
ENST00000549247.6:n.936A>T
ENST00000551114.2:n.839A>T
ENST00000553106.5:c.1177A>T ENSP00000448059.1:p.Asn393Tyr
ENST00000635477.1:c.281A>T
ENST00000635528.1:n.692A>T
NM_000277.1:c.1177A>T NP_000268.1:p.Asn393Tyr
XM_011538422.1:c.1120A>T XP_011536724.1:p.Asn374Tyr
NM_000277.2:c.1177A>T NP_000268.1:p.Asn393Tyr
NM_001354304.1:c.1177A>T NP_001341233.1:p.Asn393Tyr
NM_000277.3:c.1177A>T MANE Select NP_000268.1:p.Asn393Tyr
NM_001354304.2:c.1177A>T NP_001341233.1:p.Asn393Tyr
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