Canonical Allele Identifier: CA2059456763
Gene: PAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102866153G= , CM000674.2:g.102866153G= GRCh38
NC_000012.11:g.103259931G= , CM000674.1:g.103259931G= GRCh37
NC_000012.10:g.101784061G= NCBI36
NG_008690.1:g.56450C=
NG_008690.2:g.97258C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.509+443C= MANE Select ENSP00000448059.1:n.509+443C=
ENST00000307000.7:c.494+443C= ENSP00000303500.2:n.494+443C=
ENST00000549111.5:n.605+443C=
ENST00000551988.5:n.531-10821C=
ENST00000553106.5:c.509+443C= ENSP00000448059.1:n.509+443C=
NM_000277.1:c.509+443C= NP_000268.1:n.509+443C=
XM_011538422.1:c.509+443C= XP_011536724.1:n.509+443C=
NM_000277.2:c.509+443C= NP_000268.1:n.509+443C=
NM_001354304.1:c.509+443C= NP_001341233.1:n.509+443C=
XM_017019370.2:c.509+443C= XP_016874859.1:n.509+443C=
NM_000277.3:c.509+443C= MANE Select NP_000268.1:n.509+443C=
NM_001354304.2:c.509+443C= NP_001341233.1:n.509+443C=