Canonical Allele Identifier: CA3197755568
Community Standard Title: NM_000277.3(PAH):c.706+232T=
Gene: PAH HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102854904A= , CM000674.2:g.102854904A= GRCh38
NC_000012.11:g.103248682A= , CM000674.1:g.103248682A= GRCh37
NC_000012.10:g.101772812A= NCBI36
NG_008690.1:g.67699T=
NG_008690.2:g.108507T=

Transcript Alleles

HGVS Amino-acid Change
NM_000277.3:c.706+232T= MANE Select NP_000268.1:n.706+232T=
ENST00000553106.6:c.706+232T= MANE Select ENSP00000448059.1:n.706+232T=
NM_000277.1:c.706+232T= NP_000268.1:n.706+232T=
NM_000277.2:c.706+232T= NP_000268.1:n.706+232T=
NM_001354304.1:c.706+232T= NP_001341233.1:n.706+232T=
NM_001354304.2:c.706+232T= NP_001341233.1:n.706+232T=
ENST00000307000.7:c.691+232T= ENSP00000303500.2:n.691+232T=
ENST00000549111.5:n.1034T=
ENST00000553106.5:c.706+232T= ENSP00000448059.1:n.706+232T=
XM_011538422.1:c.706+232T= XP_011536724.1:n.706+232T=
XM_017019370.2:c.707-103T= XP_016874859.1:n.707-103T=
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