Canonical Allele Identifier: CA386493514
Gene: PAH HGNC NCBI

Linked Data

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

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

Transcript Alleles

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