Canonical Allele Identifier: CA682609243

Gene: CLEC12B

Linked Data

• dbSNP Id: rs1263817535
• gnomAD v3: 12-10017736-TAGA-T
• gnomAD v4: 12-10017736-TAGA-T
• MyVariant Identifiers: chr12:g.10170336_10170338del (hg19) ; chr12:g.10017737_10017739del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.10017737_10017739del , CM000674.2:g.10017737_10017739del	GRCh38
NC_000012.11:g.10170336_10170338del , CM000674.1:g.10170336_10170338del	GRCh37
NC_000012.10:g.10061603_10061605del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338896.11:c.681-594_681-592del MANE Select	ENSP00000344563.5:n.681-594_681-592del
ENST00000338896.10:c.681-594_681-592del	ENSP00000344563.5:n.681-594_681-592del
ENST00000338896.9:c.681-594_681-592del	ENSP00000344563.5:n.681-594_681-592del
ENST00000396502.5:c.*1991_*1993del	ENSP00000379759.1:n.*1991_*1993del
ENST00000539155.1:c.*2484_*2486del	ENSP00000444909.1:n.*2484_*2486del
ENST00000544853.5:c.*129-594_*129-592del	ENSP00000439561.1:n.*129-594_*129-592del
NM_001129998.1:c.681-594_681-592del	NP_001123470.1:n.681-594_681-592del
NM_205852.2:c.*1991_*1993del	NP_995324.2:n.*1991_*1993del
NR_120484.1:n.249-1966_249-1964del
XM_006719070.2:c.681-681_681-679del	XP_006719133.1:n.681-681_681-679del
XM_006719071.2:c.*3-594_*3-592del	XP_006719134.1:n.*3-594_*3-592del
XM_006719072.1:c.*764_*766del	XP_006719135.1:n.*764_*766del
XM_011520658.1:c.654-594_654-592del	XP_011518960.1:n.654-594_654-592del
XM_011520659.1:c.*740_*742del	XP_011518961.1:n.*740_*742del
XM_011520660.1:c.*735_*737del	XP_011518962.1:n.*735_*737del
XM_011520661.1:c.*10-594_*10-592del	XP_011518963.1:n.*10-594_*10-592del
XM_011520662.1:c.*771_*773del	XP_011518964.1:n.*771_*773del
XM_011520663.1:c.526-594_526-592del	XP_011518965.1:n.526-594_526-592del
XM_011520664.1:c.526-681_526-679del	XP_011518966.1:n.526-681_526-679del
XR_242889.3:n.956-594_956-592del
XR_931290.1:n.1717_1719del
NM_001129998.2:c.681-594_681-592del	NP_001123470.1:n.681-594_681-592del
NM_001319241.1:c.372-594_372-592del	NP_001306170.1:n.372-594_372-592del
NM_001319242.1:c.*1991_*1993del	NP_001306171.1:n.*1991_*1993del
NM_205852.3:c.*1991_*1993del	NP_995324.2:n.*1991_*1993del
NR_135049.1:n.961-594_961-592del
XM_011520658.2:c.654-594_654-592del	XP_011518960.1:n.654-594_654-592del
XM_011520663.2:c.526-594_526-592del	XP_011518965.1:n.526-594_526-592del
XM_017019295.1:c.372-594_372-592del	XP_016874784.1:n.372-594_372-592del
XM_024448976.1:c.681-681_681-679del	XP_024304744.1:n.681-681_681-679del
XM_024448977.1:c.*1998_*2000del	XP_024304745.1:n.*1998_*2000del
XR_002957401.1:n.106-1591_106-1589del
NM_001129998.3:c.681-594_681-592del MANE Select	NP_001123470.1:n.681-594_681-592del
NM_001387138.1:c.681-681_681-679del	NP_001374067.1:n.681-681_681-679del
NR_169587.1:n.258-1591_258-1589del