Canonical Allele Identifier: CA232780526

Gene: CLEC12B

Linked Data

• dbSNP Id: rs749677154
• gnomAD v2: 12-10170496-CTA-C
• gnomAD v4: 12-10017897-CTA-C
• MyVariant Identifiers: chr12:g.10170497_10170498del (hg19) ; chr12:g.10017898_10017899del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.10017899_10017900del , CM000674.2:g.10017899_10017900del	GRCh38
NC_000012.11:g.10170498_10170499del , CM000674.1:g.10170498_10170499del	GRCh37
NC_000012.10:g.10061765_10061766del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338896.11:c.681-432_681-431del MANE Select	ENSP00000344563.5:n.681-432_681-431del
ENST00000338896.10:c.681-432_681-431del	ENSP00000344563.5:n.681-432_681-431del
ENST00000338896.9:c.681-432_681-431del	ENSP00000344563.5:n.681-432_681-431del
ENST00000396502.5:c.*2153_*2154del	ENSP00000379759.1:n.*2153_*2154del
ENST00000539155.1:c.*2646_*2647del	ENSP00000444909.1:n.*2646_*2647del
ENST00000544853.5:c.*129-432_*129-431del	ENSP00000439561.1:n.*129-432_*129-431del
NM_001129998.1:c.681-432_681-431del	NP_001123470.1:n.681-432_681-431del
NM_205852.2:c.*2153_*2154del	NP_995324.2:n.*2153_*2154del
NR_120484.1:n.249-2126_249-2125del
XM_006719070.2:c.681-519_681-518del	XP_006719133.1:n.681-519_681-518del
XM_006719071.2:c.*3-432_*3-431del	XP_006719134.1:n.*3-432_*3-431del
XM_006719072.1:c.*926_*927del	XP_006719135.1:n.*926_*927del
XM_011520658.1:c.654-432_654-431del	XP_011518960.1:n.654-432_654-431del
XM_011520659.1:c.*902_*903del	XP_011518961.1:n.*902_*903del
XM_011520660.1:c.*897_*898del	XP_011518962.1:n.*897_*898del
XM_011520661.1:c.*10-432_*10-431del	XP_011518963.1:n.*10-432_*10-431del
XM_011520662.1:c.*933_*934del	XP_011518964.1:n.*933_*934del
XM_011520663.1:c.526-432_526-431del	XP_011518965.1:n.526-432_526-431del
XM_011520664.1:c.526-519_526-518del	XP_011518966.1:n.526-519_526-518del
XR_242889.3:n.956-432_956-431del
XR_931290.1:n.1879_1880del
NM_001129998.2:c.681-432_681-431del	NP_001123470.1:n.681-432_681-431del
NM_001319241.1:c.372-432_372-431del	NP_001306170.1:n.372-432_372-431del
NM_001319242.1:c.*2153_*2154del	NP_001306171.1:n.*2153_*2154del
NM_205852.3:c.*2153_*2154del	NP_995324.2:n.*2153_*2154del
NR_135049.1:n.961-432_961-431del
XM_011520658.2:c.654-432_654-431del	XP_011518960.1:n.654-432_654-431del
XM_011520663.2:c.526-432_526-431del	XP_011518965.1:n.526-432_526-431del
XM_017019295.1:c.372-432_372-431del	XP_016874784.1:n.372-432_372-431del
XM_024448976.1:c.681-519_681-518del	XP_024304744.1:n.681-519_681-518del
XM_024448977.1:c.*2160_*2161del	XP_024304745.1:n.*2160_*2161del
XR_002957401.1:n.106-1751_106-1750del
NM_001129998.3:c.681-432_681-431del MANE Select	NP_001123470.1:n.681-432_681-431del
NM_001387138.1:c.681-519_681-518del	NP_001374067.1:n.681-519_681-518del
NR_169587.1:n.258-1751_258-1750del