Canonical Allele Identifier: CA2015750727

Gene: CLEC12B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.10017759_10017760delinsTA , CM000674.2:g.10017759_10017760delinsTA	GRCh38
NC_000012.11:g.10170358_10170359delinsTA , CM000674.1:g.10170358_10170359delinsTA	GRCh37
NC_000012.10:g.10061625_10061626delinsTA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338896.11:c.681-572_681-571delinsTA MANE Select	ENSP00000344563.5:n.681-572_681-571delinsTA
ENST00000338896.10:c.681-572_681-571delinsTA	ENSP00000344563.5:n.681-572_681-571delinsTA
ENST00000338896.9:c.681-572_681-571delinsTA	ENSP00000344563.5:n.681-572_681-571delinsTA
ENST00000396502.5:c.*2013_*2014delinsTA	ENSP00000379759.1:n.*2013_*2014delinsTA
ENST00000539155.1:c.*2506_*2507delinsTA	ENSP00000444909.1:n.*2506_*2507delinsTA
ENST00000544853.5:c.*129-572_*129-571delinsTA	ENSP00000439561.1:n.*129-572_*129-571delinsTA
NM_001129998.1:c.681-572_681-571delinsTA	NP_001123470.1:n.681-572_681-571delinsTA
NM_205852.2:c.*2013_*2014delinsTA	NP_995324.2:n.*2013_*2014delinsTA
NR_120484.1:n.249-1987_249-1986delinsTA
XM_006719070.2:c.681-659_681-658delinsTA	XP_006719133.1:n.681-659_681-658delinsTA
XM_006719071.2:c.*3-572_*3-571delinsTA	XP_006719134.1:n.*3-572_*3-571delinsTA
XM_006719072.1:c.*786_*787delinsTA	XP_006719135.1:n.*786_*787delinsTA
XM_011520658.1:c.654-572_654-571delinsTA	XP_011518960.1:n.654-572_654-571delinsTA
XM_011520659.1:c.*762_*763delinsTA	XP_011518961.1:n.*762_*763delinsTA
XM_011520660.1:c.*757_*758delinsTA	XP_011518962.1:n.*757_*758delinsTA
XM_011520661.1:c.*10-572_*10-571delinsTA	XP_011518963.1:n.*10-572_*10-571delinsTA
XM_011520662.1:c.*793_*794delinsTA	XP_011518964.1:n.*793_*794delinsTA
XM_011520663.1:c.526-572_526-571delinsTA	XP_011518965.1:n.526-572_526-571delinsTA
XM_011520664.1:c.526-659_526-658delinsTA	XP_011518966.1:n.526-659_526-658delinsTA
XR_242889.3:n.956-572_956-571delinsTA
XR_931290.1:n.1739_1740delinsTA
NM_001129998.2:c.681-572_681-571delinsTA	NP_001123470.1:n.681-572_681-571delinsTA
NM_001319241.1:c.372-572_372-571delinsTA	NP_001306170.1:n.372-572_372-571delinsTA
NM_001319242.1:c.*2013_*2014delinsTA	NP_001306171.1:n.*2013_*2014delinsTA
NM_205852.3:c.*2013_*2014delinsTA	NP_995324.2:n.*2013_*2014delinsTA
NR_135049.1:n.961-572_961-571delinsTA
XM_011520658.2:c.654-572_654-571delinsTA	XP_011518960.1:n.654-572_654-571delinsTA
XM_011520663.2:c.526-572_526-571delinsTA	XP_011518965.1:n.526-572_526-571delinsTA
XM_017019295.1:c.372-572_372-571delinsTA	XP_016874784.1:n.372-572_372-571delinsTA
XM_024448976.1:c.681-659_681-658delinsTA	XP_024304744.1:n.681-659_681-658delinsTA
XM_024448977.1:c.*2020_*2021delinsTA	XP_024304745.1:n.*2020_*2021delinsTA
XR_002957401.1:n.106-1612_106-1611delinsTA
NM_001129998.3:c.681-572_681-571delinsTA MANE Select	NP_001123470.1:n.681-572_681-571delinsTA
NM_001387138.1:c.681-659_681-658delinsTA	NP_001374067.1:n.681-659_681-658delinsTA
NR_169587.1:n.258-1612_258-1611delinsTA