Canonical Allele Identifier: CA891843770

Gene: PRRT2

Linked Data

• ClinVar Variation Id: 589991
• ClinVar RCV Id: RCV002318176 ; RCV002534978
• dbSNP Id: rs1567380086
• MyVariant Identifiers: chr16:g.29825177_29825179del (hg19) ; chr16:g.29813856_29813858del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.29813856_29813858del , CM000678.2:g.29813856_29813858del	GRCh38
NC_000016.9:g.29825177_29825179del , CM000678.1:g.29825177_29825179del	GRCh37
NC_000016.8:g.29732678_29732680del	NCBI36
NG_032039.1:g.6769_6771del

Transcript Alleles

HGVS	Amino-acid change
ENST00000358758.12:c.802_804del MANE Select	ENSP00000351608.7:p.Tyr268del
ENST00000567551.2:c.339+463_339+465del	ENSP00000489813.1:n.339+463_339+465del
ENST00000636131.1:c.802_804del	ENSP00000490390.1:p.Tyr268del
ENST00000636619.1:c.724+78_724+80del	ENSP00000489669.1:n.724+78_724+80del
ENST00000637064.1:c.802_804del	ENSP00000490826.1:p.Tyr268del
ENST00000637290.1:c.*117_*119del	ENSP00000490278.1:n.*117_*119del
ENST00000637403.1:c.721+81_721+83del	ENSP00000489782.1:n.721+81_721+83del
ENST00000637565.1:c.339+463_339+465del	ENSP00000490207.1:n.339+463_339+465del
ENST00000647876.1:c.802_804del	ENSP00000498021.1:p.Tyr268del
ENST00000300797.7:c.802_804del	ENSP00000300797.6:p.Tyr268del
ENST00000358758.11:c.802_804del	ENSP00000351608.7:p.Tyr268del
ENST00000567659.3:c.802_804del	ENSP00000456226.1:p.Tyr268del
ENST00000572820.2:c.802_804del	ENSP00000458291.2:p.Tyr268del
ENST00000609618.2:c.802_804del	ENSP00000476774.2:p.Tyr268del
NM_001256442.1:c.802_804del	NP_001243371.1:p.Tyr268del
NM_001256443.1:c.802_804del	NP_001243372.1:p.Tyr268del
NM_145239.2:c.802_804del	NP_660282.2:p.Tyr268del
XM_011545715.1:c.802_804del	XP_011544017.1:p.Tyr268del
XM_011545716.1:c.802_804del	XP_011544018.1:p.Tyr268del
XM_011545717.1:c.802_804del	XP_011544019.1:p.Tyr268del
XM_011545718.1:c.802_804del	XP_011544020.1:p.Tyr268del
XM_011545715.3:c.802_804del	XP_011544017.1:p.Tyr268del
XM_017022887.2:c.802_804del	XP_016878376.1:p.Tyr268del
XM_017022888.2:c.802_804del	XP_016878377.1:p.Tyr268del
XM_017022889.2:c.802_804del	XP_016878378.1:p.Tyr268del
NM_145239.3:c.802_804del MANE Select	NP_660282.2:p.Tyr268del
NM_001256442.2:c.802_804del	NP_001243371.1:p.Tyr268del
NM_001256443.2:c.802_804del	NP_001243372.1:p.Tyr268del