Canonical Allele Identifier: CA481333638
Gene: PAH HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.103306628G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102912850G>A , CM000674.2:g.102912850G>A GRCh38
NC_000012.11:g.103306628G>A , CM000674.1:g.103306628G>A GRCh37
NC_000012.10:g.101830758G>A NCBI36
NG_008690.1:g.9753C>T
NG_008690.2:g.50561C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.109C>T MANE Select ENSP00000448059.1:p.Leu37=
ENST00000307000.7:c.94C>T ENSP00000303500.2:p.Leu32=
ENST00000546844.1:c.109C>T ENSP00000446658.1:p.Leu37=
ENST00000548677.2:n.196C>T
ENST00000548928.1:n.31C>T
ENST00000549111.5:n.205C>T
ENST00000550978.6:c.93C>T
ENST00000551337.5:c.109C>T ENSP00000447620.1:p.Leu37=
ENST00000551988.5:n.198C>T
ENST00000553106.5:c.109C>T ENSP00000448059.1:p.Leu37=
ENST00000635500.1:n.77C>T
NM_000277.1:c.109C>T NP_000268.1:p.Leu37=
XM_011538422.1:c.109C>T XP_011536724.1:p.Leu37=
NM_000277.2:c.109C>T NP_000268.1:p.Leu37=
NM_001354304.1:c.109C>T NP_001341233.1:p.Leu37=
XM_017019370.2:c.109C>T XP_016874859.1:p.Leu37=
NM_000277.3:c.109C>T MANE Select NP_000268.1:p.Leu37=
NM_001354304.2:c.109C>T NP_001341233.1:p.Leu37=