Canonical Allele Identifier: CA3197744117
Community Standard Title: NM_000277.3(PAH):c.1199+28A=
Gene: PAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102843618T= , CM000674.2:g.102843618T= GRCh38
NC_000012.11:g.103237396T= , CM000674.1:g.103237396T= GRCh37
NC_000012.10:g.101761526T= NCBI36
NG_008690.1:g.78985A=
NG_008690.2:g.119793A=

Transcript Alleles

HGVS Amino-acid Change
NM_000277.3:c.1199+28A= MANE Select NP_000268.1:n.1199+28A=
ENST00000553106.6:c.1199+28A= MANE Select ENSP00000448059.1:n.1199+28A=
NM_000277.1:c.1199+28A= NP_000268.1:n.1199+28A=
NM_000277.2:c.1199+28A= NP_000268.1:n.1199+28A=
NM_001354304.1:c.1199+28A= NP_001341233.1:n.1199+28A=
NM_001354304.2:c.1199+28A= NP_001341233.1:n.1199+28A=
ENST00000307000.7:c.1184+28A= ENSP00000303500.2:n.1184+28A=
ENST00000549247.6:n.958+28A=
ENST00000551114.2:n.861+28A=
ENST00000553106.5:c.1199+28A= ENSP00000448059.1:n.1199+28A=
ENST00000635477.1:c.303+28A=
ENST00000635528.1:n.714+28A=
XM_011538422.1:c.1142+28A= XP_011536724.1:n.1142+28A=