Canonical Allele Identifier: CA2514686294

Gene: CLEC12B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.10017890_10017895del , CM000674.2:g.10017890_10017895del	GRCh38
NC_000012.11:g.10170489_10170494del , CM000674.1:g.10170489_10170494del	GRCh37
NC_000012.10:g.10061756_10061761del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338896.11:c.681-441_681-436del MANE Select	ENSP00000344563.5:n.681-441_681-436del
ENST00000338896.10:c.681-441_681-436del	ENSP00000344563.5:n.681-441_681-436del
ENST00000338896.9:c.681-441_681-436del	ENSP00000344563.5:n.681-441_681-436del
ENST00000396502.5:c.*2144_*2149del	ENSP00000379759.1:n.*2144_*2149del
ENST00000539155.1:c.*2637_*2642del	ENSP00000444909.1:n.*2637_*2642del
ENST00000544853.5:c.*129-441_*129-436del	ENSP00000439561.1:n.*129-441_*129-436del
NM_001129998.1:c.681-441_681-436del	NP_001123470.1:n.681-441_681-436del
NM_205852.2:c.*2144_*2149del	NP_995324.2:n.*2144_*2149del
NR_120484.1:n.249-2119_249-2114del
XM_006719070.2:c.681-528_681-523del	XP_006719133.1:n.681-528_681-523del
XM_006719071.2:c.*3-441_*3-436del	XP_006719134.1:n.*3-441_*3-436del
XM_006719072.1:c.*917_*922del	XP_006719135.1:n.*917_*922del
XM_011520658.1:c.654-441_654-436del	XP_011518960.1:n.654-441_654-436del
XM_011520659.1:c.*893_*898del	XP_011518961.1:n.*893_*898del
XM_011520660.1:c.*888_*893del	XP_011518962.1:n.*888_*893del
XM_011520661.1:c.*10-441_*10-436del	XP_011518963.1:n.*10-441_*10-436del
XM_011520662.1:c.*924_*929del	XP_011518964.1:n.*924_*929del
XM_011520663.1:c.526-441_526-436del	XP_011518965.1:n.526-441_526-436del
XM_011520664.1:c.526-528_526-523del	XP_011518966.1:n.526-528_526-523del
XR_242889.3:n.956-441_956-436del
XR_931290.1:n.1870_1875del
NM_001129998.2:c.681-441_681-436del	NP_001123470.1:n.681-441_681-436del
NM_001319241.1:c.372-441_372-436del	NP_001306170.1:n.372-441_372-436del
NM_001319242.1:c.*2144_*2149del	NP_001306171.1:n.*2144_*2149del
NM_205852.3:c.*2144_*2149del	NP_995324.2:n.*2144_*2149del
NR_135049.1:n.961-441_961-436del
XM_011520658.2:c.654-441_654-436del	XP_011518960.1:n.654-441_654-436del
XM_011520663.2:c.526-441_526-436del	XP_011518965.1:n.526-441_526-436del
XM_017019295.1:c.372-441_372-436del	XP_016874784.1:n.372-441_372-436del
XM_024448976.1:c.681-528_681-523del	XP_024304744.1:n.681-528_681-523del
XM_024448977.1:c.*2151_*2156del	XP_024304745.1:n.*2151_*2156del
XR_002957401.1:n.106-1744_106-1739del
NM_001129998.3:c.681-441_681-436del MANE Select	NP_001123470.1:n.681-441_681-436del
NM_001387138.1:c.681-528_681-523del	NP_001374067.1:n.681-528_681-523del
NR_169587.1:n.258-1744_258-1739del