Canonical Allele Identifier: CA2059448619
Gene: PAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102844438T= , CM000674.2:g.102844438T= GRCh38
NC_000012.11:g.103238216T= , CM000674.1:g.103238216T= GRCh37
NC_000012.10:g.101762346T= NCBI36
NG_008690.1:g.78165A=
NG_008690.2:g.118973A=

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.970-7A= MANE Select ENSP00000448059.1:n.970-7A=
ENST00000307000.7:c.955-7A= ENSP00000303500.2:n.955-7A=
ENST00000549247.6:n.729-7A=
ENST00000551114.2:n.632-7A=
ENST00000553106.5:c.970-7A= ENSP00000448059.1:n.970-7A=
ENST00000635477.1:c.74-7A=
ENST00000635528.1:n.485-7A=
NM_000277.1:c.970-7A= NP_000268.1:n.970-7A=
XM_011538422.1:c.913-7A= XP_011536724.1:n.913-7A=
NM_000277.2:c.970-7A= NP_000268.1:n.970-7A=
NM_001354304.1:c.970-7A= NP_001341233.1:n.970-7A=
NM_000277.3:c.970-7A= MANE Select NP_000268.1:n.970-7A=
NM_001354304.2:c.970-7A= NP_001341233.1:n.970-7A=