Canonical Allele Identifier: CA2560228023

Gene: CLEC12B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.10017883_10017884insA , CM000674.2:g.10017883_10017884insA	GRCh38
NC_000012.11:g.10170482_10170483insA , CM000674.1:g.10170482_10170483insA	GRCh37
NC_000012.10:g.10061749_10061750insA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338896.11:c.681-448_681-447insA MANE Select	ENSP00000344563.5:n.681-448_681-447insA
ENST00000338896.10:c.681-448_681-447insA	ENSP00000344563.5:n.681-448_681-447insA
ENST00000338896.9:c.681-448_681-447insA	ENSP00000344563.5:n.681-448_681-447insA
ENST00000396502.5:c.*2137_*2138insA	ENSP00000379759.1:n.*2137_*2138insA
ENST00000539155.1:c.*2630_*2631insA	ENSP00000444909.1:n.*2630_*2631insA
ENST00000544853.5:c.*129-448_*129-447insA	ENSP00000439561.1:n.*129-448_*129-447insA
NM_001129998.1:c.681-448_681-447insA	NP_001123470.1:n.681-448_681-447insA
NM_205852.2:c.*2137_*2138insA	NP_995324.2:n.*2137_*2138insA
NR_120484.1:n.249-2111_249-2110insT
XM_006719070.2:c.681-535_681-534insA	XP_006719133.1:n.681-535_681-534insA
XM_006719071.2:c.*3-448_*3-447insA	XP_006719134.1:n.*3-448_*3-447insA
XM_006719072.1:c.*910_*911insA	XP_006719135.1:n.*910_*911insA
XM_011520658.1:c.654-448_654-447insA	XP_011518960.1:n.654-448_654-447insA
XM_011520659.1:c.*886_*887insA	XP_011518961.1:n.*886_*887insA
XM_011520660.1:c.*881_*882insA	XP_011518962.1:n.*881_*882insA
XM_011520661.1:c.*10-448_*10-447insA	XP_011518963.1:n.*10-448_*10-447insA
XM_011520662.1:c.*917_*918insA	XP_011518964.1:n.*917_*918insA
XM_011520663.1:c.526-448_526-447insA	XP_011518965.1:n.526-448_526-447insA
XM_011520664.1:c.526-535_526-534insA	XP_011518966.1:n.526-535_526-534insA
XR_242889.3:n.956-448_956-447insA
XR_931290.1:n.1863_1864insA
NM_001129998.2:c.681-448_681-447insA	NP_001123470.1:n.681-448_681-447insA
NM_001319241.1:c.372-448_372-447insA	NP_001306170.1:n.372-448_372-447insA
NM_001319242.1:c.*2137_*2138insA	NP_001306171.1:n.*2137_*2138insA
NM_205852.3:c.*2137_*2138insA	NP_995324.2:n.*2137_*2138insA
NR_135049.1:n.961-448_961-447insA
XM_011520658.2:c.654-448_654-447insA	XP_011518960.1:n.654-448_654-447insA
XM_011520663.2:c.526-448_526-447insA	XP_011518965.1:n.526-448_526-447insA
XM_017019295.1:c.372-448_372-447insA	XP_016874784.1:n.372-448_372-447insA
XM_024448976.1:c.681-535_681-534insA	XP_024304744.1:n.681-535_681-534insA
XM_024448977.1:c.*2144_*2145insA	XP_024304745.1:n.*2144_*2145insA
XR_002957401.1:n.106-1736_106-1735insT
NM_001129998.3:c.681-448_681-447insA MANE Select	NP_001123470.1:n.681-448_681-447insA
NM_001387138.1:c.681-535_681-534insA	NP_001374067.1:n.681-535_681-534insA
NR_169587.1:n.258-1736_258-1735insT