Canonical Allele Identifier: CA232780420

Gene: CLEC12B

Linked Data

• dbSNP Id: rs766397647
• gnomAD v3: 12-10017824-CATATCT-C
• gnomAD v4: 12-10017824-CATATCT-C
• MyVariant Identifiers: chr12:g.10170424_10170429del (hg19) ; chr12:g.10017825_10017830del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.10017829_10017834del , CM000674.2:g.10017829_10017834del	GRCh38
NC_000012.11:g.10170428_10170433del , CM000674.1:g.10170428_10170433del	GRCh37
NC_000012.10:g.10061695_10061700del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338896.11:c.681-502_681-497del MANE Select	ENSP00000344563.5:n.681-502_681-497del
ENST00000338896.10:c.681-502_681-497del	ENSP00000344563.5:n.681-502_681-497del
ENST00000338896.9:c.681-502_681-497del	ENSP00000344563.5:n.681-502_681-497del
ENST00000396502.5:c.*2083_*2088del	ENSP00000379759.1:n.*2083_*2088del
ENST00000539155.1:c.*2576_*2581del	ENSP00000444909.1:n.*2576_*2581del
ENST00000544853.5:c.*129-502_*129-497del	ENSP00000439561.1:n.*129-502_*129-497del
NM_001129998.1:c.681-502_681-497del	NP_001123470.1:n.681-502_681-497del
NM_205852.2:c.*2083_*2088del	NP_995324.2:n.*2083_*2088del
NR_120484.1:n.249-2057_249-2052del
XM_006719070.2:c.681-589_681-584del	XP_006719133.1:n.681-589_681-584del
XM_006719071.2:c.*3-502_*3-497del	XP_006719134.1:n.*3-502_*3-497del
XM_006719072.1:c.*856_*861del	XP_006719135.1:n.*856_*861del
XM_011520658.1:c.654-502_654-497del	XP_011518960.1:n.654-502_654-497del
XM_011520659.1:c.*832_*837del	XP_011518961.1:n.*832_*837del
XM_011520660.1:c.*827_*832del	XP_011518962.1:n.*827_*832del
XM_011520661.1:c.*10-502_*10-497del	XP_011518963.1:n.*10-502_*10-497del
XM_011520662.1:c.*863_*868del	XP_011518964.1:n.*863_*868del
XM_011520663.1:c.526-502_526-497del	XP_011518965.1:n.526-502_526-497del
XM_011520664.1:c.526-589_526-584del	XP_011518966.1:n.526-589_526-584del
XR_242889.3:n.956-502_956-497del
XR_931290.1:n.1809_1814del
NM_001129998.2:c.681-502_681-497del	NP_001123470.1:n.681-502_681-497del
NM_001319241.1:c.372-502_372-497del	NP_001306170.1:n.372-502_372-497del
NM_001319242.1:c.*2083_*2088del	NP_001306171.1:n.*2083_*2088del
NM_205852.3:c.*2083_*2088del	NP_995324.2:n.*2083_*2088del
NR_135049.1:n.961-502_961-497del
XM_011520658.2:c.654-502_654-497del	XP_011518960.1:n.654-502_654-497del
XM_011520663.2:c.526-502_526-497del	XP_011518965.1:n.526-502_526-497del
XM_017019295.1:c.372-502_372-497del	XP_016874784.1:n.372-502_372-497del
XM_024448976.1:c.681-589_681-584del	XP_024304744.1:n.681-589_681-584del
XM_024448977.1:c.*2090_*2095del	XP_024304745.1:n.*2090_*2095del
XR_002957401.1:n.106-1682_106-1677del
NM_001129998.3:c.681-502_681-497del MANE Select	NP_001123470.1:n.681-502_681-497del
NM_001387138.1:c.681-589_681-584del	NP_001374067.1:n.681-589_681-584del
NR_169587.1:n.258-1682_258-1677del