Canonical Allele Identifier: CA10603377

Gene: PRRT2

Linked Data

• ClinVar Variation Id: 280549
• ClinVar RCV Id: RCV000311228
• dbSNP Id: rs886041735
• MyVariant Identifiers: chr16:g.29824566_29824582dup17 (hg19) ; chr16:g.29813245_29813261dup17 (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.29813245_29813261dup , CM000678.2:g.29813245_29813261dup	GRCh38
NC_000016.9:g.29824566_29824582dup , CM000678.1:g.29824566_29824582dup	GRCh37
NC_000016.8:g.29732067_29732083dup	NCBI36
NG_032039.1:g.6158_6174dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358758.12:c.191_207dup MANE Select	ENSP00000351608.7:p.Glu70ArgfsTer26
ENST00000567551.2:c.191_207dup	ENSP00000489813.1:p.Glu70ArgfsTer26
ENST00000636019.1:n.88-441_88-425dup
ENST00000636131.1:c.191_207dup	ENSP00000490390.1:p.Glu70ArgfsTer26
ENST00000636246.1:c.191_207dup	ENSP00000489948.1:p.Glu70ArgfsTer26
ENST00000636619.1:c.191_207dup	ENSP00000489669.1:p.Glu70ArgfsTer26
ENST00000637064.1:c.191_207dup	ENSP00000490826.1:p.Glu70ArgfsTer26
ENST00000637290.1:c.191_207dup	ENSP00000490278.1:p.Glu70ArgfsTer26
ENST00000637403.1:c.191_207dup	ENSP00000489782.1:p.Glu70ArgfsTer26
ENST00000637565.1:c.191_207dup	ENSP00000490207.1:p.Glu70ArgfsTer26
ENST00000637596.1:c.191_207dup	ENSP00000489805.1:p.Glu70ArgfsTer26
ENST00000647876.1:c.191_207dup	ENSP00000498021.1:p.Glu70ArgfsTer26
ENST00000300797.7:c.191_207dup	ENSP00000300797.6:p.Glu70ArgfsTer26
ENST00000358758.11:c.191_207dup	ENSP00000351608.7:p.Glu70ArgfsTer26
ENST00000562148.2:c.191_207dup	ENSP00000454634.2:p.Glu70ArgfsTer26
ENST00000567551.1:n.304_320dup
ENST00000567659.3:c.191_207dup	ENSP00000456226.1:p.Glu70ArgfsTer26
ENST00000572820.2:c.191_207dup	ENSP00000458291.2:p.Glu70ArgfsTer26
ENST00000609618.2:c.191_207dup	ENSP00000476774.2:p.Glu70ArgfsTer26
NM_001256442.1:c.191_207dup	NP_001243371.1:p.Glu70ArgfsTer26
NM_001256443.1:c.191_207dup	NP_001243372.1:p.Glu70ArgfsTer26
NM_145239.2:c.191_207dup	NP_660282.2:p.Glu70ArgfsTer26
XM_011545715.1:c.191_207dup	XP_011544017.1:p.Glu70ArgfsTer26
XM_011545716.1:c.191_207dup	XP_011544018.1:p.Glu70ArgfsTer26
XM_011545717.1:c.191_207dup	XP_011544019.1:p.Glu70ArgfsTer26
XM_011545718.1:c.191_207dup	XP_011544020.1:p.Glu70ArgfsTer26
XM_011545715.3:c.191_207dup	XP_011544017.1:p.Glu70ArgfsTer26
XM_017022887.2:c.191_207dup	XP_016878376.1:p.Glu70ArgfsTer26
XM_017022888.2:c.191_207dup	XP_016878377.1:p.Glu70ArgfsTer26
XM_017022889.2:c.191_207dup	XP_016878378.1:p.Glu70ArgfsTer26
NM_145239.3:c.191_207dup MANE Select	NP_660282.2:p.Glu70ArgfsTer26
NM_001256442.2:c.191_207dup	NP_001243371.1:p.Glu70ArgfsTer26
NM_001256443.2:c.191_207dup	NP_001243372.1:p.Glu70ArgfsTer26