Canonical Allele Identifier: CA944652592

Gene: CLEC12B

Linked Data

• dbSNP Id: rs1865526132
• gnomAD v3: 12-10017860-C-CTGTCTTGT
• gnomAD v4: 12-10017860-C-CTGTCTTGT

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.10017862_10017869dup , CM000674.2:g.10017862_10017869dup	GRCh38
NC_000012.11:g.10170461_10170468dup , CM000674.1:g.10170461_10170468dup	GRCh37
NC_000012.10:g.10061728_10061735dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338896.11:c.681-469_681-462dup MANE Select	ENSP00000344563.5:n.681-469_681-462dup
ENST00000338896.10:c.681-469_681-462dup	ENSP00000344563.5:n.681-469_681-462dup
ENST00000338896.9:c.681-469_681-462dup	ENSP00000344563.5:n.681-469_681-462dup
ENST00000396502.5:c.*2116_*2123dup	ENSP00000379759.1:n.*2116_*2123dup
ENST00000539155.1:c.*2609_*2616dup	ENSP00000444909.1:n.*2609_*2616dup
ENST00000544853.5:c.*129-469_*129-462dup	ENSP00000439561.1:n.*129-469_*129-462dup
NM_001129998.1:c.681-469_681-462dup	NP_001123470.1:n.681-469_681-462dup
NM_205852.2:c.*2116_*2123dup	NP_995324.2:n.*2116_*2123dup
NR_120484.1:n.249-2095_249-2088dup
XM_006719070.2:c.681-556_681-549dup	XP_006719133.1:n.681-556_681-549dup
XM_006719071.2:c.*3-469_*3-462dup	XP_006719134.1:n.*3-469_*3-462dup
XM_006719072.1:c.*889_*896dup	XP_006719135.1:n.*889_*896dup
XM_011520658.1:c.654-469_654-462dup	XP_011518960.1:n.654-469_654-462dup
XM_011520659.1:c.*865_*872dup	XP_011518961.1:n.*865_*872dup
XM_011520660.1:c.*860_*867dup	XP_011518962.1:n.*860_*867dup
XM_011520661.1:c.*10-469_*10-462dup	XP_011518963.1:n.*10-469_*10-462dup
XM_011520662.1:c.*896_*903dup	XP_011518964.1:n.*896_*903dup
XM_011520663.1:c.526-469_526-462dup	XP_011518965.1:n.526-469_526-462dup
XM_011520664.1:c.526-556_526-549dup	XP_011518966.1:n.526-556_526-549dup
XR_242889.3:n.956-469_956-462dup
XR_931290.1:n.1842_1849dup
NM_001129998.2:c.681-469_681-462dup	NP_001123470.1:n.681-469_681-462dup
NM_001319241.1:c.372-469_372-462dup	NP_001306170.1:n.372-469_372-462dup
NM_001319242.1:c.*2116_*2123dup	NP_001306171.1:n.*2116_*2123dup
NM_205852.3:c.*2116_*2123dup	NP_995324.2:n.*2116_*2123dup
NR_135049.1:n.961-469_961-462dup
XM_011520658.2:c.654-469_654-462dup	XP_011518960.1:n.654-469_654-462dup
XM_011520663.2:c.526-469_526-462dup	XP_011518965.1:n.526-469_526-462dup
XM_017019295.1:c.372-469_372-462dup	XP_016874784.1:n.372-469_372-462dup
XM_024448976.1:c.681-556_681-549dup	XP_024304744.1:n.681-556_681-549dup
XM_024448977.1:c.*2123_*2130dup	XP_024304745.1:n.*2123_*2130dup
XR_002957401.1:n.106-1720_106-1713dup
NM_001129998.3:c.681-469_681-462dup MANE Select	NP_001123470.1:n.681-469_681-462dup
NM_001387138.1:c.681-556_681-549dup	NP_001374067.1:n.681-556_681-549dup
NR_169587.1:n.258-1720_258-1713dup