Canonical Allele Identifier: CA2059462488
Gene: PAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102877518C= , CM000674.2:g.102877518C= GRCh38
NC_000012.11:g.103271296C= , CM000674.1:g.103271296C= GRCh37
NC_000012.10:g.101795426C= NCBI36
NG_008690.1:g.45085G=
NG_008690.2:g.85893G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.385G= MANE Select ENSP00000448059.1:p.Asp129=
ENST00000307000.7:c.370G= ENSP00000303500.2:p.Asp124=
ENST00000549111.5:n.481G=
ENST00000550978.6:c.369G=
ENST00000551337.5:c.385G= ENSP00000447620.1:p.Asp129=
ENST00000551988.5:n.474G=
ENST00000553106.5:c.385G= ENSP00000448059.1:p.Asp129=
NM_000277.1:c.385G= NP_000268.1:p.Asp129=
XM_011538422.1:c.385G= XP_011536724.1:p.Asp129=
NM_000277.2:c.385G= NP_000268.1:p.Asp129=
NM_001354304.1:c.385G= NP_001341233.1:p.Asp129=
XM_017019370.2:c.385G= XP_016874859.1:p.Asp129=
NM_000277.3:c.385G= MANE Select NP_000268.1:p.Asp129=
NM_001354304.2:c.385G= NP_001341233.1:p.Asp129=