Canonical Allele Identifier: CA2059442381
Gene: PAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102840666T= , CM000674.2:g.102840666T= GRCh38
NC_000012.11:g.103234444T= , CM000674.1:g.103234444T= GRCh37
NC_000012.10:g.101758574T= NCBI36
NG_008690.1:g.81937A=
NG_008690.2:g.122745A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.1200-151A= MANE Select ENSP00000448059.1:n.1200-151A=
ENST00000307000.7:c.1185-151A= ENSP00000303500.2:n.1185-151A=
ENST00000549247.6:n.959-151A=
ENST00000551114.2:n.862-151A=
ENST00000553106.5:c.1200-151A= ENSP00000448059.1:n.1200-151A=
ENST00000635477.1:c.304-151A=
ENST00000635528.1:n.715-151A=
NM_000277.1:c.1200-151A= NP_000268.1:n.1200-151A=
XM_011538422.1:c.1143-151A= XP_011536724.1:n.1143-151A=
NM_000277.2:c.1200-151A= NP_000268.1:n.1200-151A=
NM_001354304.1:c.1200-151A= NP_001341233.1:n.1200-151A=
NM_000277.3:c.1200-151A= MANE Select NP_000268.1:n.1200-151A=
NM_001354304.2:c.1200-151A= NP_001341233.1:n.1200-151A=