Canonical Allele Identifier: CA2015750751

Gene: CLEC12B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.10017824_10017830delinsCATATCT , CM000674.2:g.10017824_10017830delinsCATATCT	GRCh38
NC_000012.11:g.10170423_10170429delinsCATATCT , CM000674.1:g.10170423_10170429delinsCATATCT	GRCh37
NC_000012.10:g.10061690_10061696delinsCATATCT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338896.11:c.681-507_681-501delinsCATATCT MANE Select	ENSP00000344563.5:n.681-507_681-501delinsCATATCT
ENST00000338896.10:c.681-507_681-501delinsCATATCT	ENSP00000344563.5:n.681-507_681-501delinsCATATCT
ENST00000338896.9:c.681-507_681-501delinsCATATCT	ENSP00000344563.5:n.681-507_681-501delinsCATATCT
ENST00000396502.5:c.*2078_*2084delinsCATATCT	ENSP00000379759.1:n.*2078_*2084delinsCATATCT
ENST00000539155.1:c.*2571_*2577delinsCATATCT	ENSP00000444909.1:n.*2571_*2577delinsCATATCT
ENST00000544853.5:c.*129-507_*129-501delinsCATATCT	ENSP00000439561.1:n.*129-507_*129-501delinsCATATCT
NM_001129998.1:c.681-507_681-501delinsCATATCT	NP_001123470.1:n.681-507_681-501delinsCATATCT
NM_205852.2:c.*2078_*2084delinsCATATCT	NP_995324.2:n.*2078_*2084delinsCATATCT
NR_120484.1:n.249-2057_249-2051delinsAGATATG
XM_006719070.2:c.681-594_681-588delinsCATATCT	XP_006719133.1:n.681-594_681-588delinsCATATCT
XM_006719071.2:c.*3-507_*3-501delinsCATATCT	XP_006719134.1:n.*3-507_*3-501delinsCATATCT
XM_006719072.1:c.*851_*857delinsCATATCT	XP_006719135.1:n.*851_*857delinsCATATCT
XM_011520658.1:c.654-507_654-501delinsCATATCT	XP_011518960.1:n.654-507_654-501delinsCATATCT
XM_011520659.1:c.*827_*833delinsCATATCT	XP_011518961.1:n.*827_*833delinsCATATCT
XM_011520660.1:c.*822_*828delinsCATATCT	XP_011518962.1:n.*822_*828delinsCATATCT
XM_011520661.1:c.*10-507_*10-501delinsCATATCT	XP_011518963.1:n.*10-507_*10-501delinsCATATCT
XM_011520662.1:c.*858_*864delinsCATATCT	XP_011518964.1:n.*858_*864delinsCATATCT
XM_011520663.1:c.526-507_526-501delinsCATATCT	XP_011518965.1:n.526-507_526-501delinsCATATCT
XM_011520664.1:c.526-594_526-588delinsCATATCT	XP_011518966.1:n.526-594_526-588delinsCATATCT
XR_242889.3:n.956-507_956-501delinsCATATCT
XR_931290.1:n.1804_1810delinsCATATCT
NM_001129998.2:c.681-507_681-501delinsCATATCT	NP_001123470.1:n.681-507_681-501delinsCATATCT
NM_001319241.1:c.372-507_372-501delinsCATATCT	NP_001306170.1:n.372-507_372-501delinsCATATCT
NM_001319242.1:c.*2078_*2084delinsCATATCT	NP_001306171.1:n.*2078_*2084delinsCATATCT
NM_205852.3:c.*2078_*2084delinsCATATCT	NP_995324.2:n.*2078_*2084delinsCATATCT
NR_135049.1:n.961-507_961-501delinsCATATCT
XM_011520658.2:c.654-507_654-501delinsCATATCT	XP_011518960.1:n.654-507_654-501delinsCATATCT
XM_011520663.2:c.526-507_526-501delinsCATATCT	XP_011518965.1:n.526-507_526-501delinsCATATCT
XM_017019295.1:c.372-507_372-501delinsCATATCT	XP_016874784.1:n.372-507_372-501delinsCATATCT
XM_024448976.1:c.681-594_681-588delinsCATATCT	XP_024304744.1:n.681-594_681-588delinsCATATCT
XM_024448977.1:c.*2085_*2091delinsCATATCT	XP_024304745.1:n.*2085_*2091delinsCATATCT
XR_002957401.1:n.106-1682_106-1676delinsAGATATG
NM_001129998.3:c.681-507_681-501delinsCATATCT MANE Select	NP_001123470.1:n.681-507_681-501delinsCATATCT
NM_001387138.1:c.681-594_681-588delinsCATATCT	NP_001374067.1:n.681-594_681-588delinsCATATCT
NR_169587.1:n.258-1682_258-1676delinsAGATATG