Canonical Allele Identifier: CA386493513
Gene: PAH HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.103238201C>A (hg19) chr12:g.102844423C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102844423C>A , CM000674.2:g.102844423C>A GRCh38
NC_000012.11:g.103238201C>A , CM000674.1:g.103238201C>A GRCh37
NC_000012.10:g.101762331C>A NCBI36
NG_008690.1:g.78180G>T
NG_008690.2:g.118988G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.978G>T MANE Select ENSP00000448059.1:p.Trp326Cys
ENST00000307000.7:c.963G>T ENSP00000303500.2:p.Trp321Cys
ENST00000549247.6:n.737G>T
ENST00000551114.2:n.640G>T
ENST00000553106.5:c.978G>T ENSP00000448059.1:p.Trp326Cys
ENST00000635477.1:c.82G>T
ENST00000635528.1:n.493G>T
NM_000277.1:c.978G>T NP_000268.1:p.Trp326Cys
XM_011538422.1:c.921G>T XP_011536724.1:p.Trp307Cys
NM_000277.2:c.978G>T NP_000268.1:p.Trp326Cys
NM_001354304.1:c.978G>T NP_001341233.1:p.Trp326Cys
NM_000277.3:c.978G>T MANE Select NP_000268.1:p.Trp326Cys
NM_001354304.2:c.978G>T NP_001341233.1:p.Trp326Cys
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