Canonical Allele Identifier: CA2617597568

Gene: CLEC12B

Linked Data

• gnomAD v4: 12-10017519-T-TACAG

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.10017522_10017525dup , CM000674.2:g.10017522_10017525dup	GRCh38
NC_000012.11:g.10170121_10170124dup , CM000674.1:g.10170121_10170124dup	GRCh37
NC_000012.10:g.10061388_10061391dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338896.11:c.681-809_681-806dup MANE Select	ENSP00000344563.5:n.681-809_681-806dup
ENST00000338896.10:c.681-809_681-806dup	ENSP00000344563.5:n.681-809_681-806dup
ENST00000338896.9:c.681-809_681-806dup	ENSP00000344563.5:n.681-809_681-806dup
ENST00000396502.5:c.*1776_*1779dup	ENSP00000379759.1:n.*1776_*1779dup
ENST00000539155.1:c.*2269_*2272dup	ENSP00000444909.1:n.*2269_*2272dup
ENST00000544853.5:c.*129-809_*129-806dup	ENSP00000439561.1:n.*129-809_*129-806dup
NM_001129998.1:c.681-809_681-806dup	NP_001123470.1:n.681-809_681-806dup
NM_205852.2:c.*1776_*1779dup	NP_995324.2:n.*1776_*1779dup
NR_120484.1:n.249-1750_249-1747dup
XM_006719070.2:c.681-896_681-893dup	XP_006719133.1:n.681-896_681-893dup
XM_006719071.2:c.*3-809_*3-806dup	XP_006719134.1:n.*3-809_*3-806dup
XM_006719072.1:c.*549_*552dup	XP_006719135.1:n.*549_*552dup
XM_011520658.1:c.654-809_654-806dup	XP_011518960.1:n.654-809_654-806dup
XM_011520659.1:c.*525_*528dup	XP_011518961.1:n.*525_*528dup
XM_011520660.1:c.*520_*523dup	XP_011518962.1:n.*520_*523dup
XM_011520661.1:c.*10-809_*10-806dup	XP_011518963.1:n.*10-809_*10-806dup
XM_011520662.1:c.*556_*559dup	XP_011518964.1:n.*556_*559dup
XM_011520663.1:c.526-809_526-806dup	XP_011518965.1:n.526-809_526-806dup
XM_011520664.1:c.526-896_526-893dup	XP_011518966.1:n.526-896_526-893dup
XR_242889.3:n.956-809_956-806dup
XR_931290.1:n.1502_1505dup
NM_001129998.2:c.681-809_681-806dup	NP_001123470.1:n.681-809_681-806dup
NM_001319241.1:c.372-809_372-806dup	NP_001306170.1:n.372-809_372-806dup
NM_001319242.1:c.*1776_*1779dup	NP_001306171.1:n.*1776_*1779dup
NM_205852.3:c.*1776_*1779dup	NP_995324.2:n.*1776_*1779dup
NR_135049.1:n.961-809_961-806dup
XM_011520658.2:c.654-809_654-806dup	XP_011518960.1:n.654-809_654-806dup
XM_011520663.2:c.526-809_526-806dup	XP_011518965.1:n.526-809_526-806dup
XM_017019295.1:c.372-809_372-806dup	XP_016874784.1:n.372-809_372-806dup
XM_024448976.1:c.681-896_681-893dup	XP_024304744.1:n.681-896_681-893dup
XM_024448977.1:c.*1783_*1786dup	XP_024304745.1:n.*1783_*1786dup
XR_002957401.1:n.106-1375_106-1372dup
NM_001129998.3:c.681-809_681-806dup MANE Select	NP_001123470.1:n.681-809_681-806dup
NM_001387138.1:c.681-896_681-893dup	NP_001374067.1:n.681-896_681-893dup
NR_169587.1:n.258-1375_258-1372dup