Canonical Allele Identifier: CA2015750777

Gene: CLEC12B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.10017871_10017872delinsTC , CM000674.2:g.10017871_10017872delinsTC	GRCh38
NC_000012.11:g.10170470_10170471delinsTC , CM000674.1:g.10170470_10170471delinsTC	GRCh37
NC_000012.10:g.10061737_10061738delinsTC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338896.11:c.681-460_681-459delinsTC MANE Select	ENSP00000344563.5:n.681-460_681-459delinsTC
ENST00000338896.10:c.681-460_681-459delinsTC	ENSP00000344563.5:n.681-460_681-459delinsTC
ENST00000338896.9:c.681-460_681-459delinsTC	ENSP00000344563.5:n.681-460_681-459delinsTC
ENST00000396502.5:c.*2125_*2126delinsTC	ENSP00000379759.1:n.*2125_*2126delinsTC
ENST00000539155.1:c.*2618_*2619delinsTC	ENSP00000444909.1:n.*2618_*2619delinsTC
ENST00000544853.5:c.*129-460_*129-459delinsTC	ENSP00000439561.1:n.*129-460_*129-459delinsTC
NM_001129998.1:c.681-460_681-459delinsTC	NP_001123470.1:n.681-460_681-459delinsTC
NM_205852.2:c.*2125_*2126delinsTC	NP_995324.2:n.*2125_*2126delinsTC
NR_120484.1:n.249-2099_249-2098delinsGA
XM_006719070.2:c.681-547_681-546delinsTC	XP_006719133.1:n.681-547_681-546delinsTC
XM_006719071.2:c.*3-460_*3-459delinsTC	XP_006719134.1:n.*3-460_*3-459delinsTC
XM_006719072.1:c.*898_*899delinsTC	XP_006719135.1:n.*898_*899delinsTC
XM_011520658.1:c.654-460_654-459delinsTC	XP_011518960.1:n.654-460_654-459delinsTC
XM_011520659.1:c.*874_*875delinsTC	XP_011518961.1:n.*874_*875delinsTC
XM_011520660.1:c.*869_*870delinsTC	XP_011518962.1:n.*869_*870delinsTC
XM_011520661.1:c.*10-460_*10-459delinsTC	XP_011518963.1:n.*10-460_*10-459delinsTC
XM_011520662.1:c.*905_*906delinsTC	XP_011518964.1:n.*905_*906delinsTC
XM_011520663.1:c.526-460_526-459delinsTC	XP_011518965.1:n.526-460_526-459delinsTC
XM_011520664.1:c.526-547_526-546delinsTC	XP_011518966.1:n.526-547_526-546delinsTC
XR_242889.3:n.956-460_956-459delinsTC
XR_931290.1:n.1851_1852delinsTC
NM_001129998.2:c.681-460_681-459delinsTC	NP_001123470.1:n.681-460_681-459delinsTC
NM_001319241.1:c.372-460_372-459delinsTC	NP_001306170.1:n.372-460_372-459delinsTC
NM_001319242.1:c.*2125_*2126delinsTC	NP_001306171.1:n.*2125_*2126delinsTC
NM_205852.3:c.*2125_*2126delinsTC	NP_995324.2:n.*2125_*2126delinsTC
NR_135049.1:n.961-460_961-459delinsTC
XM_011520658.2:c.654-460_654-459delinsTC	XP_011518960.1:n.654-460_654-459delinsTC
XM_011520663.2:c.526-460_526-459delinsTC	XP_011518965.1:n.526-460_526-459delinsTC
XM_017019295.1:c.372-460_372-459delinsTC	XP_016874784.1:n.372-460_372-459delinsTC
XM_024448976.1:c.681-547_681-546delinsTC	XP_024304744.1:n.681-547_681-546delinsTC
XM_024448977.1:c.*2132_*2133delinsTC	XP_024304745.1:n.*2132_*2133delinsTC
XR_002957401.1:n.106-1724_106-1723delinsGA
NM_001129998.3:c.681-460_681-459delinsTC MANE Select	NP_001123470.1:n.681-460_681-459delinsTC
NM_001387138.1:c.681-547_681-546delinsTC	NP_001374067.1:n.681-547_681-546delinsTC
NR_169587.1:n.258-1724_258-1723delinsGA