Canonical Allele Identifier: CA2571991687

Gene: RFX8

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.101412762_101412763insTGAGGGG , CM000664.2:g.101412762_101412763insTGAGGGG	GRCh38
NC_000002.11:g.102029224_102029225insTGAGGGG , CM000664.1:g.102029224_102029225insTGAGGGG	GRCh37
NC_000002.10:g.101395656_101395657insTGAGGGG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646893.2:c.1057+152_1057+153insCCCCTCA	ENSP00000494249.2:n.1057+152_1057+153insCCCCTCA
ENST00000428343.6:c.718+152_718+153insCCCCTCA MANE Select	ENSP00000401536.1:n.718+152_718+153insCCCCTCA
ENST00000646446.1:c.931+152_931+153insCCCCTCA	ENSP00000494216.1:n.931+152_931+153insCCCCTCA
ENST00000646893.1:c.844+152_844+153insCCCCTCA	ENSP00000494249.1:n.844+152_844+153insCCCCTCA
ENST00000428343.5:c.718+152_718+153insCCCCTCA	ENSP00000401536.1:n.718+152_718+153insCCCCTCA
ENST00000481179.5:c.*434+152_*434+153insCCCCTCA	ENSP00000422968.1:n.*434+152_*434+153insCCCCTCA
NM_001145664.1:c.718+152_718+153insCCCCTCA	NP_001139136.1:n.718+152_718+153insCCCCTCA
XM_011511771.1:c.946+152_946+153insCCCCTCA	XP_011510073.1:n.946+152_946+153insCCCCTCA
XM_011511772.1:c.931+152_931+153insCCCCTCA	XP_011510074.1:n.931+152_931+153insCCCCTCA
XM_011511773.1:c.628+152_628+153insCCCCTCA	XP_011510075.1:n.628+152_628+153insCCCCTCA
XM_011511774.1:c.946+152_946+153insCCCCTCA	XP_011510076.1:n.946+152_946+153insCCCCTCA
XM_011511775.1:c.946+152_946+153insCCCCTCA	XP_011510077.1:n.946+152_946+153insCCCCTCA
XM_011511776.1:c.430+152_430+153insCCCCTCA	XP_011510078.1:n.430+152_430+153insCCCCTCA
XM_011511777.1:c.430+152_430+153insCCCCTCA	XP_011510079.1:n.430+152_430+153insCCCCTCA
XM_011511778.1:c.430+152_430+153insCCCCTCA	XP_011510080.1:n.430+152_430+153insCCCCTCA
XM_011511771.2:c.946+152_946+153insCCCCTCA	XP_011510073.1:n.946+152_946+153insCCCCTCA
XM_011511777.2:c.430+152_430+153insCCCCTCA	XP_011510079.1:n.430+152_430+153insCCCCTCA
XM_017004851.1:c.1057+152_1057+153insCCCCTCA	XP_016860340.1:n.1057+152_1057+153insCCCCTCA
XM_017004852.1:c.844+152_844+153insCCCCTCA	XP_016860341.1:n.844+152_844+153insCCCCTCA
XM_017004853.1:c.1057+152_1057+153insCCCCTCA	XP_016860342.1:n.1057+152_1057+153insCCCCTCA
XM_017004854.1:c.1057+152_1057+153insCCCCTCA	XP_016860343.1:n.1057+152_1057+153insCCCCTCA
XR_001738924.1:n.1001+152_1001+153insCCCCTCA
NM_001145664.2:c.718+152_718+153insCCCCTCA MANE Select	NP_001139136.2:n.718+152_718+153insCCCCTCA
NM_001367508.1:c.205+152_205+153insCCCCTCA	NP_001354437.1:n.205+152_205+153insCCCCTCA
NM_001367509.1:c.205+152_205+153insCCCCTCA	NP_001354438.1:n.205+152_205+153insCCCCTCA
NM_001367510.1:c.205+152_205+153insCCCCTCA	NP_001354439.1:n.205+152_205+153insCCCCTCA