Canonical Allele Identifier: CA386492937
Gene: PAH HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.103234190C>A (hg19) chr12:g.102840412C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102840412C>A , CM000674.2:g.102840412C>A GRCh38
NC_000012.11:g.103234190C>A , CM000674.1:g.103234190C>A GRCh37
NC_000012.10:g.101758320C>A NCBI36
NG_008690.1:g.82191G>T
NG_008690.2:g.122999G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.1303G>T MANE Select ENSP00000448059.1:p.Asp435Tyr
ENST00000307000.7:c.1288G>T ENSP00000303500.2:p.Asp430Tyr
ENST00000551114.2:n.965G>T
ENST00000553106.5:c.1303G>T ENSP00000448059.1:p.Asp435Tyr
ENST00000635477.1:c.407G>T
ENST00000635528.1:n.818G>T
NM_000277.1:c.1303G>T NP_000268.1:p.Asp435Tyr
XM_011538422.1:c.1246G>T XP_011536724.1:p.Asp416Tyr
NM_000277.2:c.1303G>T NP_000268.1:p.Asp435Tyr
NM_001354304.1:c.1303G>T NP_001341233.1:p.Asp435Tyr
NM_000277.3:c.1303G>T MANE Select NP_000268.1:p.Asp435Tyr
NM_001354304.2:c.1303G>T NP_001341233.1:p.Asp435Tyr
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