Canonical Allele Identifier: CA481375323
Gene: PAH HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.103234182A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102840404A>T , CM000674.2:g.102840404A>T GRCh38
NC_000012.11:g.103234182A>T , CM000674.1:g.103234182A>T GRCh37
NC_000012.10:g.101758312A>T NCBI36
NG_008690.1:g.82199T>A
NG_008690.2:g.123007T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.1311T>A MANE Select ENSP00000448059.1:p.Ile437=
ENST00000307000.7:c.1296T>A ENSP00000303500.2:p.Ile432=
ENST00000551114.2:n.973T>A
ENST00000553106.5:c.1311T>A ENSP00000448059.1:p.Ile437=
ENST00000635477.1:n.415T>A
ENST00000635528.1:n.826T>A
NM_000277.1:c.1311T>A NP_000268.1:p.Ile437=
XM_011538422.1:c.1254T>A XP_011536724.1:p.Ile418=
NM_000277.2:c.1311T>A NP_000268.1:p.Ile437=
NM_001354304.1:c.1311T>A NP_001341233.1:p.Ile437=
NM_000277.3:c.1311T>A MANE Select NP_000268.1:p.Ile437=
NM_001354304.2:c.1311T>A NP_001341233.1:p.Ile437=