Canonical Allele Identifier: CA2059448929
Gene: PAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102844626C= , CM000674.2:g.102844626C= GRCh38
NC_000012.11:g.103238404C= , CM000674.1:g.103238404C= GRCh37
NC_000012.10:g.101762534C= NCBI36
NG_008690.1:g.77977G=
NG_008690.2:g.118785G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.970-195G= MANE Select ENSP00000448059.1:n.970-195G=
ENST00000307000.7:c.955-195G= ENSP00000303500.2:n.955-195G=
ENST00000549247.6:n.729-195G=
ENST00000551114.2:n.632-195G=
ENST00000553106.5:c.970-195G= ENSP00000448059.1:n.970-195G=
ENST00000635477.1:c.74-195G=
ENST00000635528.1:n.485-195G=
NM_000277.1:c.970-195G= NP_000268.1:n.970-195G=
XM_011538422.1:c.913-195G= XP_011536724.1:n.913-195G=
NM_000277.2:c.970-195G= NP_000268.1:n.970-195G=
NM_001354304.1:c.970-195G= NP_001341233.1:n.970-195G=
NM_000277.3:c.970-195G= MANE Select NP_000268.1:n.970-195G=
NM_001354304.2:c.970-195G= NP_001341233.1:n.970-195G=