Canonical Allele Identifier: CA603258189

Gene: CLEC12B

Linked Data

• dbSNP Id: rs1399057639
• gnomAD v2: 12-10170066-CACTCTT-C
• gnomAD v4: 12-10017467-CACTCTT-C
• MyVariant Identifiers: chr12:g.10170067_10170072del (hg19) ; chr12:g.10017468_10017473del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.10017469_10017474del , CM000674.2:g.10017469_10017474del	GRCh38
NC_000012.11:g.10170068_10170073del , CM000674.1:g.10170068_10170073del	GRCh37
NC_000012.10:g.10061335_10061340del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000338896.11:c.681-862_681-857del MANE Select	ENSP00000344563.5:n.681-862_681-857del
ENST00000338896.10:c.681-862_681-857del	ENSP00000344563.5:n.681-862_681-857del
ENST00000338896.9:c.681-862_681-857del	ENSP00000344563.5:n.681-862_681-857del
ENST00000396502.5:c.*1723_*1728del	ENSP00000379759.1:n.*1723_*1728del
ENST00000539155.1:c.*2216_*2221del	ENSP00000444909.1:n.*2216_*2221del
ENST00000544853.5:c.*129-862_*129-857del	ENSP00000439561.1:n.*129-862_*129-857del
NM_001129998.1:c.681-862_681-857del	NP_001123470.1:n.681-862_681-857del
NM_205852.2:c.*1723_*1728del	NP_995324.2:n.*1723_*1728del
NR_120484.1:n.249-1700_249-1695del
XM_006719070.2:c.681-949_681-944del	XP_006719133.1:n.681-949_681-944del
XM_006719071.2:c.*3-862_*3-857del	XP_006719134.1:n.*3-862_*3-857del
XM_006719072.1:c.*496_*501del	XP_006719135.1:n.*496_*501del
XM_011520658.1:c.654-862_654-857del	XP_011518960.1:n.654-862_654-857del
XM_011520659.1:c.*472_*477del	XP_011518961.1:n.*472_*477del
XM_011520660.1:c.*467_*472del	XP_011518962.1:n.*467_*472del
XM_011520661.1:c.*10-862_*10-857del	XP_011518963.1:n.*10-862_*10-857del
XM_011520662.1:c.*503_*508del	XP_011518964.1:n.*503_*508del
XM_011520663.1:c.526-862_526-857del	XP_011518965.1:n.526-862_526-857del
XM_011520664.1:c.526-949_526-944del	XP_011518966.1:n.526-949_526-944del
XR_242889.3:n.956-862_956-857del
XR_931290.1:n.1449_1454del
NM_001129998.2:c.681-862_681-857del	NP_001123470.1:n.681-862_681-857del
NM_001319241.1:c.372-862_372-857del	NP_001306170.1:n.372-862_372-857del
NM_001319242.1:c.*1723_*1728del	NP_001306171.1:n.*1723_*1728del
NM_205852.3:c.*1723_*1728del	NP_995324.2:n.*1723_*1728del
NR_135049.1:n.961-862_961-857del
XM_011520658.2:c.654-862_654-857del	XP_011518960.1:n.654-862_654-857del
XM_011520663.2:c.526-862_526-857del	XP_011518965.1:n.526-862_526-857del
XM_017019295.1:c.372-862_372-857del	XP_016874784.1:n.372-862_372-857del
XM_024448976.1:c.681-949_681-944del	XP_024304744.1:n.681-949_681-944del
XM_024448977.1:c.*1730_*1735del	XP_024304745.1:n.*1730_*1735del
XR_002957401.1:n.106-1325_106-1320del
NM_001129998.3:c.681-862_681-857del MANE Select	NP_001123470.1:n.681-862_681-857del
NM_001387138.1:c.681-949_681-944del	NP_001374067.1:n.681-949_681-944del
NR_169587.1:n.258-1325_258-1320del