Canonical Allele Identifier: CA1274778761

Gene: RFX8

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.101413338_101413354delinsCAATCGCCCCACGCCCA , CM000664.2:g.101413338_101413354delinsCAATCGCCCCACGCCCA	GRCh38
NC_000002.11:g.102029800_102029816delinsCAATCGCCCCACGCCCA , CM000664.1:g.102029800_102029816delinsCAATCGCCCCACGCCCA	GRCh37
NC_000002.10:g.101396232_101396248delinsCAATCGCCCCACGCCCA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646893.2:c.901-283_901-267delinsTGGGCGTGGGGCGATTG	ENSP00000494249.2:n.901-283_901-267delinsTGGGCGTGGGGCGATTG
ENST00000428343.6:c.562-283_562-267delinsTGGGCGTGGGGCGATTG MANE Select	ENSP00000401536.1:n.562-283_562-267delinsTGGGCGTGGGGCGATTG
ENST00000646446.1:c.775-283_775-267delinsTGGGCGTGGGGCGATTG	ENSP00000494216.1:n.775-283_775-267delinsTGGGCGTGGGGCGATTG
ENST00000646893.1:c.688-283_688-267delinsTGGGCGTGGGGCGATTG	ENSP00000494249.1:n.688-283_688-267delinsTGGGCGTGGGGCGATTG
ENST00000428343.5:c.562-283_562-267delinsTGGGCGTGGGGCGATTG	ENSP00000401536.1:n.562-283_562-267delinsTGGGCGTGGGGCGATTG
ENST00000481179.5:c.*278-283_*278-267delinsTGGGCGTGGGGCGATTG	ENSP00000422968.1:n.*278-283_*278-267delinsTGGGCGTGGGGCGATTG
NM_001145664.1:c.562-283_562-267delinsTGGGCGTGGGGCGATTG	NP_001139136.1:n.562-283_562-267delinsTGGGCGTGGGGCGATTG
XM_011511771.1:c.790-283_790-267delinsTGGGCGTGGGGCGATTG	XP_011510073.1:n.790-283_790-267delinsTGGGCGTGGGGCGATTG
XM_011511772.1:c.775-283_775-267delinsTGGGCGTGGGGCGATTG	XP_011510074.1:n.775-283_775-267delinsTGGGCGTGGGGCGATTG
XM_011511773.1:c.472-283_472-267delinsTGGGCGTGGGGCGATTG	XP_011510075.1:n.472-283_472-267delinsTGGGCGTGGGGCGATTG
XM_011511774.1:c.790-283_790-267delinsTGGGCGTGGGGCGATTG	XP_011510076.1:n.790-283_790-267delinsTGGGCGTGGGGCGATTG
XM_011511775.1:c.790-283_790-267delinsTGGGCGTGGGGCGATTG	XP_011510077.1:n.790-283_790-267delinsTGGGCGTGGGGCGATTG
XM_011511776.1:c.274-283_274-267delinsTGGGCGTGGGGCGATTG	XP_011510078.1:n.274-283_274-267delinsTGGGCGTGGGGCGATTG
XM_011511777.1:c.274-283_274-267delinsTGGGCGTGGGGCGATTG	XP_011510079.1:n.274-283_274-267delinsTGGGCGTGGGGCGATTG
XM_011511778.1:c.274-283_274-267delinsTGGGCGTGGGGCGATTG	XP_011510080.1:n.274-283_274-267delinsTGGGCGTGGGGCGATTG
XM_011511779.1:c.731-283_731-267delinsTGGGCGTGGGGCGATTG	XP_011510081.1:n.731-283_731-267delinsTGGGCGTGGGGCGATTG
XM_011511771.2:c.790-283_790-267delinsTGGGCGTGGGGCGATTG	XP_011510073.1:n.790-283_790-267delinsTGGGCGTGGGGCGATTG
XM_011511777.2:c.274-283_274-267delinsTGGGCGTGGGGCGATTG	XP_011510079.1:n.274-283_274-267delinsTGGGCGTGGGGCGATTG
XM_017004851.1:c.901-283_901-267delinsTGGGCGTGGGGCGATTG	XP_016860340.1:n.901-283_901-267delinsTGGGCGTGGGGCGATTG
XM_017004852.1:c.688-283_688-267delinsTGGGCGTGGGGCGATTG	XP_016860341.1:n.688-283_688-267delinsTGGGCGTGGGGCGATTG
XM_017004853.1:c.901-283_901-267delinsTGGGCGTGGGGCGATTG	XP_016860342.1:n.901-283_901-267delinsTGGGCGTGGGGCGATTG
XM_017004854.1:c.901-283_901-267delinsTGGGCGTGGGGCGATTG	XP_016860343.1:n.901-283_901-267delinsTGGGCGTGGGGCGATTG
XR_001738924.1:n.845-283_845-267delinsTGGGCGTGGGGCGATTG
NM_001145664.2:c.562-283_562-267delinsTGGGCGTGGGGCGATTG MANE Select	NP_001139136.2:n.562-283_562-267delinsTGGGCGTGGGGCGATTG
NM_001367508.1:c.49-283_49-267delinsTGGGCGTGGGGCGATTG	NP_001354437.1:n.49-283_49-267delinsTGGGCGTGGGGCGATTG
NM_001367509.1:c.49-283_49-267delinsTGGGCGTGGGGCGATTG	NP_001354438.1:n.49-283_49-267delinsTGGGCGTGGGGCGATTG
NM_001367510.1:c.49-283_49-267delinsTGGGCGTGGGGCGATTG	NP_001354439.1:n.49-283_49-267delinsTGGGCGTGGGGCGATTG