Canonical Allele Identifier: CA2015750706

Gene: CLEC12B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.10017708_10017713delinsAAAAAC , CM000674.2:g.10017708_10017713delinsAAAAAC	GRCh38
NC_000012.11:g.10170307_10170312delinsAAAAAC , CM000674.1:g.10170307_10170312delinsAAAAAC	GRCh37
NC_000012.10:g.10061574_10061579delinsAAAAAC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338896.11:c.681-623_681-618delinsAAAAAC MANE Select	ENSP00000344563.5:n.681-623_681-618delinsAAAAAC
ENST00000338896.10:c.681-623_681-618delinsAAAAAC	ENSP00000344563.5:n.681-623_681-618delinsAAAAAC
ENST00000338896.9:c.681-623_681-618delinsAAAAAC	ENSP00000344563.5:n.681-623_681-618delinsAAAAAC
ENST00000396502.5:c.*1962_*1967delinsAAAAAC	ENSP00000379759.1:n.*1962_*1967delinsAAAAAC
ENST00000539155.1:c.*2455_*2460delinsAAAAAC	ENSP00000444909.1:n.*2455_*2460delinsAAAAAC
ENST00000544853.5:c.*129-623_*129-618delinsAAAAAC	ENSP00000439561.1:n.*129-623_*129-618delinsAAAAAC
NM_001129998.1:c.681-623_681-618delinsAAAAAC	NP_001123470.1:n.681-623_681-618delinsAAAAAC
NM_205852.2:c.*1962_*1967delinsAAAAAC	NP_995324.2:n.*1962_*1967delinsAAAAAC
NR_120484.1:n.249-1940_249-1935delinsGTTTTT
XM_006719070.2:c.681-710_681-705delinsAAAAAC	XP_006719133.1:n.681-710_681-705delinsAAAAAC
XM_006719071.2:c.*3-623_*3-618delinsAAAAAC	XP_006719134.1:n.*3-623_*3-618delinsAAAAAC
XM_006719072.1:c.*735_*740delinsAAAAAC	XP_006719135.1:n.*735_*740delinsAAAAAC
XM_011520658.1:c.654-623_654-618delinsAAAAAC	XP_011518960.1:n.654-623_654-618delinsAAAAAC
XM_011520659.1:c.*711_*716delinsAAAAAC	XP_011518961.1:n.*711_*716delinsAAAAAC
XM_011520660.1:c.*706_*711delinsAAAAAC	XP_011518962.1:n.*706_*711delinsAAAAAC
XM_011520661.1:c.*10-623_*10-618delinsAAAAAC	XP_011518963.1:n.*10-623_*10-618delinsAAAAAC
XM_011520662.1:c.*742_*747delinsAAAAAC	XP_011518964.1:n.*742_*747delinsAAAAAC
XM_011520663.1:c.526-623_526-618delinsAAAAAC	XP_011518965.1:n.526-623_526-618delinsAAAAAC
XM_011520664.1:c.526-710_526-705delinsAAAAAC	XP_011518966.1:n.526-710_526-705delinsAAAAAC
XR_242889.3:n.956-623_956-618delinsAAAAAC
XR_931290.1:n.1688_1693delinsAAAAAC
NM_001129998.2:c.681-623_681-618delinsAAAAAC	NP_001123470.1:n.681-623_681-618delinsAAAAAC
NM_001319241.1:c.372-623_372-618delinsAAAAAC	NP_001306170.1:n.372-623_372-618delinsAAAAAC
NM_001319242.1:c.*1962_*1967delinsAAAAAC	NP_001306171.1:n.*1962_*1967delinsAAAAAC
NM_205852.3:c.*1962_*1967delinsAAAAAC	NP_995324.2:n.*1962_*1967delinsAAAAAC
NR_135049.1:n.961-623_961-618delinsAAAAAC
XM_011520658.2:c.654-623_654-618delinsAAAAAC	XP_011518960.1:n.654-623_654-618delinsAAAAAC
XM_011520663.2:c.526-623_526-618delinsAAAAAC	XP_011518965.1:n.526-623_526-618delinsAAAAAC
XM_017019295.1:c.372-623_372-618delinsAAAAAC	XP_016874784.1:n.372-623_372-618delinsAAAAAC
XM_024448976.1:c.681-710_681-705delinsAAAAAC	XP_024304744.1:n.681-710_681-705delinsAAAAAC
XM_024448977.1:c.*1969_*1974delinsAAAAAC	XP_024304745.1:n.*1969_*1974delinsAAAAAC
XR_002957401.1:n.106-1565_106-1560delinsGTTTTT
NM_001129998.3:c.681-623_681-618delinsAAAAAC MANE Select	NP_001123470.1:n.681-623_681-618delinsAAAAAC
NM_001387138.1:c.681-710_681-705delinsAAAAAC	NP_001374067.1:n.681-710_681-705delinsAAAAAC
NR_169587.1:n.258-1565_258-1560delinsGTTTTT