Canonical Allele Identifier: CA645595365
Gene: PRRT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.29813701_29813703del , CM000678.2:g.29813701_29813703del GRCh38
NC_000016.9:g.29825022_29825024del , CM000678.1:g.29825022_29825024del GRCh37
NC_000016.8:g.29732523_29732525del NCBI36
NG_032039.1:g.6614_6616del

Transcript Alleles

HGVS Amino-acid change
ENST00000358758.12:c.647_649del MANE Select ENSP00000351608.7:p.Pro216del
ENST00000567551.2:c.339+308_339+310del ENSP00000489813.1:n.339+308_339+310del
ENST00000636019.1:n.103_105del
ENST00000636131.1:c.647_649del ENSP00000490390.1:p.Pro216del
ENST00000636619.1:c.647_649del ENSP00000489669.1:p.Pro216del
ENST00000637064.1:c.647_649del ENSP00000490826.1:p.Pro216del
ENST00000637290.1:c.355_357del ENSP00000490278.1:p.Pro119del
ENST00000637403.1:c.647_649del ENSP00000489782.1:p.Pro216del
ENST00000637565.1:c.339+308_339+310del ENSP00000490207.1:n.339+308_339+310del
ENST00000647876.1:c.647_649del ENSP00000498021.1:p.Pro216del
ENST00000300797.7:c.647_649del ENSP00000300797.6:p.Pro216del
ENST00000358758.11:c.647_649del ENSP00000351608.7:p.Pro216del
ENST00000567551.1:n.468_470del
ENST00000567659.3:c.647_649del ENSP00000456226.1:p.Pro216del
ENST00000572820.2:c.647_649del ENSP00000458291.2:p.Pro216del
ENST00000609618.2:c.647_649del ENSP00000476774.2:p.Pro216del
NM_001256442.1:c.647_649del NP_001243371.1:p.Pro216del
NM_001256443.1:c.647_649del NP_001243372.1:p.Pro216del
NM_145239.2:c.647_649del NP_660282.2:p.Pro216del
XM_011545715.1:c.647_649del XP_011544017.1:p.Pro216del
XM_011545716.1:c.647_649del XP_011544018.1:p.Pro216del
XM_011545717.1:c.647_649del XP_011544019.1:p.Pro216del
XM_011545718.1:c.647_649del XP_011544020.1:p.Pro216del
XM_011545715.3:c.647_649del XP_011544017.1:p.Pro216del
XM_017022887.2:c.647_649del XP_016878376.1:p.Pro216del
XM_017022888.2:c.647_649del XP_016878377.1:p.Pro216del
XM_017022889.2:c.647_649del XP_016878378.1:p.Pro216del
NM_145239.3:c.647_649del MANE Select NP_660282.2:p.Pro216del
NM_001256442.2:c.647_649del NP_001243371.1:p.Pro216del
NM_001256443.2:c.647_649del NP_001243372.1:p.Pro216del