Canonical Allele Identifier: CA259999
Gene: PRRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 31177
ClinVar RCV Id: RCV000024176
dbSNP Id: rs387907128

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.29813850C>T , CM000678.2:g.29813850C>T GRCh38
NC_000016.9:g.29825171C>T , CM000678.1:g.29825171C>T GRCh37
NC_000016.8:g.29732672C>T NCBI36
NG_032039.1:g.6763C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000300797.7:c.796C>T ENSP00000300797.6:p.Arg266Trp
ENST00000358758.11:c.796C>T ENSP00000351608.7:p.Arg266Trp
ENST00000567659.3:c.796C>T ENSP00000456226.1:p.Arg266Trp
ENST00000572820.2:c.796C>T ENSP00000458291.2:p.Arg266Trp
ENST00000609618.2:c.796C>T ENSP00000476774.2:p.Arg266Trp
NM_001256442.1:c.796C>T NP_001243371.1:p.Arg266Trp
NM_001256443.1:c.796C>T NP_001243372.1:p.Arg266Trp
NM_145239.2:c.796C>T NP_660282.2:p.Arg266Trp
XM_011545715.1:c.796C>T XP_011544017.1:p.Arg266Trp
XM_011545716.1:c.796C>T XP_011544018.1:p.Arg266Trp
XM_011545717.1:c.796C>T XP_011544019.1:p.Arg266Trp
XM_011545718.1:c.796C>T XP_011544020.1:p.Arg266Trp
XM_011545715.3:c.796C>T XP_011544017.1:p.Arg266Trp
XM_017022887.2:c.796C>T XP_016878376.1:p.Arg266Trp
XM_017022888.2:c.796C>T XP_016878377.1:p.Arg266Trp
XM_017022889.2:c.796C>T XP_016878378.1:p.Arg266Trp
NM_145239.3:c.796C>T MANE Select NP_660282.2:p.Arg266Trp
NM_001256442.2:c.796C>T NP_001243371.1:p.Arg266Trp
NM_001256443.2:c.796C>T NP_001243372.1:p.Arg266Trp