Canonical Allele Identifier: CA2216294398

Gene: PRRT2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.29814146_29814148delinsAAC , CM000678.2:g.29814146_29814148delinsAAC	GRCh38
NC_000016.9:g.29825467_29825469delinsAAC , CM000678.1:g.29825467_29825469delinsAAC	GRCh37
NC_000016.8:g.29732968_29732970delinsAAC	NCBI36
NG_032039.1:g.7059_7061delinsAAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358758.12:c.880-187_880-185delinsAAC MANE Select	ENSP00000351608.7:n.880-187_880-185delinsAAC
ENST00000567551.2:c.340-187_340-185delinsAAC	ENSP00000489813.1:n.340-187_340-185delinsAAC
ENST00000636131.1:c.*55+137_*55+139delinsAAC	ENSP00000490390.1:n.*55+137_*55+139delinsAAC
ENST00000636619.1:c.725-187_725-185delinsAAC	ENSP00000489669.1:n.725-187_725-185delinsAAC
ENST00000637064.1:c.880-187_880-185delinsAAC	ENSP00000490826.1:n.880-187_880-185delinsAAC
ENST00000637290.1:c.*195-187_*195-185delinsAAC	ENSP00000490278.1:n.*195-187_*195-185delinsAAC
ENST00000637403.1:c.722-187_722-185delinsAAC	ENSP00000489782.1:n.722-187_722-185delinsAAC
ENST00000637565.1:c.340-198_340-196delinsAAC	ENSP00000490207.1:n.340-198_340-196delinsAAC
ENST00000647876.1:c.*192_*194delinsAAC	ENSP00000498021.1:n.*192_*194delinsAAC
ENST00000300797.7:c.*192_*194delinsAAC	ENSP00000300797.6:n.*192_*194delinsAAC
ENST00000358758.11:c.880-187_880-185delinsAAC	ENSP00000351608.7:n.880-187_880-185delinsAAC
ENST00000567659.3:c.880-187_880-185delinsAAC	ENSP00000456226.1:n.880-187_880-185delinsAAC
ENST00000572820.2:c.880-187_880-185delinsAAC	ENSP00000458291.2:n.880-187_880-185delinsAAC
ENST00000609618.2:c.880-198_880-196delinsAAC	ENSP00000476774.2:n.880-198_880-196delinsAAC
NM_001256442.1:c.880-187_880-185delinsAAC	NP_001243371.1:n.880-187_880-185delinsAAC
NM_001256443.1:c.*192_*194delinsAAC	NP_001243372.1:n.*192_*194delinsAAC
NM_145239.2:c.880-187_880-185delinsAAC	NP_660282.2:n.880-187_880-185delinsAAC
XM_011545715.1:c.880-187_880-185delinsAAC	XP_011544017.1:n.880-187_880-185delinsAAC
XM_011545716.1:c.880-187_880-185delinsAAC	XP_011544018.1:n.880-187_880-185delinsAAC
XM_011545717.1:c.880-187_880-185delinsAAC	XP_011544019.1:n.880-187_880-185delinsAAC
XM_011545718.1:c.880-187_880-185delinsAAC	XP_011544020.1:n.880-187_880-185delinsAAC
XM_011545715.3:c.880-187_880-185delinsAAC	XP_011544017.1:n.880-187_880-185delinsAAC
XM_017022887.2:c.880-187_880-185delinsAAC	XP_016878376.1:n.880-187_880-185delinsAAC
XM_017022888.2:c.880-187_880-185delinsAAC	XP_016878377.1:n.880-187_880-185delinsAAC
XM_017022889.2:c.880-187_880-185delinsAAC	XP_016878378.1:n.880-187_880-185delinsAAC
NM_145239.3:c.880-187_880-185delinsAAC MANE Select	NP_660282.2:n.880-187_880-185delinsAAC
NM_001256442.2:c.880-187_880-185delinsAAC	NP_001243371.1:n.880-187_880-185delinsAAC
NM_001256443.2:c.*192_*194delinsAAC	NP_001243372.1:n.*192_*194delinsAAC