Canonical Allele Identifier: CA2620525459
Community Standard Title: NM_000277.3(PAH):c.706+350G>T
Gene: PAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102854786C>A , CM000674.2:g.102854786C>A GRCh38
NC_000012.11:g.103248564C>A , CM000674.1:g.103248564C>A GRCh37
NC_000012.10:g.101772694C>A NCBI36
NG_008690.1:g.67817G>T
NG_008690.2:g.108625G>T

Transcript Alleles

HGVS Amino-acid Change
NM_000277.3:c.706+350G>T MANE Select NP_000268.1:n.706+350G>T
ENST00000553106.6:c.706+350G>T MANE Select ENSP00000448059.1:n.706+350G>T
NM_000277.1:c.706+350G>T NP_000268.1:n.706+350G>T
NM_000277.2:c.706+350G>T NP_000268.1:n.706+350G>T
NM_001354304.1:c.706+350G>T NP_001341233.1:n.706+350G>T
NM_001354304.2:c.706+350G>T NP_001341233.1:n.706+350G>T
ENST00000307000.7:c.691+350G>T ENSP00000303500.2:n.691+350G>T
ENST00000549111.5:n.1152G>T
ENST00000553106.5:c.706+350G>T ENSP00000448059.1:n.706+350G>T
XM_011538422.1:c.706+350G>T XP_011536724.1:n.706+350G>T
XM_017019370.2:c.722G>T XP_016874859.1:p.Ter241Leu