Canonical Allele Identifier: CA481578565
Gene: PAH HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.103249029C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102855251C>T , CM000674.2:g.102855251C>T GRCh38
NC_000012.11:g.103249029C>T , CM000674.1:g.103249029C>T GRCh37
NC_000012.10:g.101773159C>T NCBI36
NG_008690.1:g.67352G>A
NG_008690.2:g.108160G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.591G>A MANE Select ENSP00000448059.1:p.Leu197=
ENST00000307000.7:c.576G>A ENSP00000303500.2:p.Leu192=
ENST00000549111.5:n.687G>A
ENST00000553106.5:c.591G>A ENSP00000448059.1:p.Leu197=
NM_000277.1:c.591G>A NP_000268.1:p.Leu197=
XM_011538422.1:c.591G>A XP_011536724.1:p.Leu197=
NM_000277.2:c.591G>A NP_000268.1:p.Leu197=
NM_001354304.1:c.591G>A NP_001341233.1:p.Leu197=
XM_017019370.2:c.591G>A XP_016874859.1:p.Leu197=
NM_000277.3:c.591G>A MANE Select NP_000268.1:p.Leu197=
NM_001354304.2:c.591G>A NP_001341233.1:p.Leu197=