Canonical Allele Identifier: CA2216294341

Gene: PRRT2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.29814030C= , CM000678.2:g.29814030C=	GRCh38
NC_000016.9:g.29825351C= , CM000678.1:g.29825351C=	GRCh37
NC_000016.8:g.29732852C=	NCBI36
NG_032039.1:g.6943C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358758.12:c.879+97C= MANE Select	ENSP00000351608.7:n.879+97C=
ENST00000567551.2:c.340-303C=	ENSP00000489813.1:n.340-303C=
ENST00000636131.1:c.*55+21C=	ENSP00000490390.1:n.*55+21C=
ENST00000636619.1:c.724+252C=	ENSP00000489669.1:n.724+252C=
ENST00000637064.1:c.879+97C=	ENSP00000490826.1:n.879+97C=
ENST00000637290.1:c.*194+97C=	ENSP00000490278.1:n.*194+97C=
ENST00000637403.1:c.721+255C=	ENSP00000489782.1:n.721+255C=
ENST00000637565.1:c.340-314C=	ENSP00000490207.1:n.340-314C=
ENST00000647876.1:c.*76C=	ENSP00000498021.1:n.*76C=
ENST00000300797.7:c.*76C=	ENSP00000300797.6:n.*76C=
ENST00000358758.11:c.879+97C=	ENSP00000351608.7:n.879+97C=
ENST00000567659.3:c.879+97C=	ENSP00000456226.1:n.879+97C=
ENST00000572820.2:c.879+97C=	ENSP00000458291.2:n.879+97C=
ENST00000609618.2:c.879+97C=	ENSP00000476774.2:n.879+97C=
NM_001256442.1:c.879+97C=	NP_001243371.1:n.879+97C=
NM_001256443.1:c.*76C=	NP_001243372.1:n.*76C=
NM_145239.2:c.879+97C=	NP_660282.2:n.879+97C=
XM_011545715.1:c.879+97C=	XP_011544017.1:n.879+97C=
XM_011545716.1:c.879+97C=	XP_011544018.1:n.879+97C=
XM_011545717.1:c.879+97C=	XP_011544019.1:n.879+97C=
XM_011545718.1:c.879+97C=	XP_011544020.1:n.879+97C=
XM_011545715.3:c.879+97C=	XP_011544017.1:n.879+97C=
XM_017022887.2:c.879+97C=	XP_016878376.1:n.879+97C=
XM_017022888.2:c.879+97C=	XP_016878377.1:n.879+97C=
XM_017022889.2:c.879+97C=	XP_016878378.1:n.879+97C=
NM_145239.3:c.879+97C= MANE Select	NP_660282.2:n.879+97C=
NM_001256442.2:c.879+97C=	NP_001243371.1:n.879+97C=
NM_001256443.2:c.*76C=	NP_001243372.1:n.*76C=