Canonical Allele Identifier: CA2059462322
Gene: PAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102877209A= , CM000674.2:g.102877209A= GRCh38
NC_000012.11:g.103270987A= , CM000674.1:g.103270987A= GRCh37
NC_000012.10:g.101795117A= NCBI36
NG_008690.1:g.45394T=
NG_008690.2:g.86202T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.441+253T= MANE Select ENSP00000448059.1:n.441+253T=
ENST00000307000.7:c.426+253T= ENSP00000303500.2:n.426+253T=
ENST00000549111.5:n.537+253T=
ENST00000551988.5:n.530+253T=
ENST00000553106.5:c.441+253T= ENSP00000448059.1:n.441+253T=
NM_000277.1:c.441+253T= NP_000268.1:n.441+253T=
XM_011538422.1:c.441+253T= XP_011536724.1:n.441+253T=
NM_000277.2:c.441+253T= NP_000268.1:n.441+253T=
NM_001354304.1:c.441+253T= NP_001341233.1:n.441+253T=
XM_017019370.2:c.441+253T= XP_016874859.1:n.441+253T=
NM_000277.3:c.441+253T= MANE Select NP_000268.1:n.441+253T=
NM_001354304.2:c.441+253T= NP_001341233.1:n.441+253T=