Canonical Allele Identifier: CA2059448607
Gene: PAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102844437A= , CM000674.2:g.102844437A= GRCh38
NC_000012.11:g.103238215A= , CM000674.1:g.103238215A= GRCh37
NC_000012.10:g.101762345A= NCBI36
NG_008690.1:g.78166T=
NG_008690.2:g.118974T=

Transcript Alleles

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