Canonical Allele Identifier: CA2015750793

Gene: CLEC12B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.10017897_10017899delinsCTA , CM000674.2:g.10017897_10017899delinsCTA	GRCh38
NC_000012.11:g.10170496_10170498delinsCTA , CM000674.1:g.10170496_10170498delinsCTA	GRCh37
NC_000012.10:g.10061763_10061765delinsCTA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338896.11:c.681-434_681-432delinsCTA MANE Select	ENSP00000344563.5:n.681-434_681-432delinsCTA
ENST00000338896.10:c.681-434_681-432delinsCTA	ENSP00000344563.5:n.681-434_681-432delinsCTA
ENST00000338896.9:c.681-434_681-432delinsCTA	ENSP00000344563.5:n.681-434_681-432delinsCTA
ENST00000396502.5:c.*2151_*2153delinsCTA	ENSP00000379759.1:n.*2151_*2153delinsCTA
ENST00000539155.1:c.*2644_*2646delinsCTA	ENSP00000444909.1:n.*2644_*2646delinsCTA
ENST00000544853.5:c.*129-434_*129-432delinsCTA	ENSP00000439561.1:n.*129-434_*129-432delinsCTA
NM_001129998.1:c.681-434_681-432delinsCTA	NP_001123470.1:n.681-434_681-432delinsCTA
NM_205852.2:c.*2151_*2153delinsCTA	NP_995324.2:n.*2151_*2153delinsCTA
NR_120484.1:n.249-2126_249-2124delinsTAG
XM_006719070.2:c.681-521_681-519delinsCTA	XP_006719133.1:n.681-521_681-519delinsCTA
XM_006719071.2:c.*3-434_*3-432delinsCTA	XP_006719134.1:n.*3-434_*3-432delinsCTA
XM_006719072.1:c.*924_*926delinsCTA	XP_006719135.1:n.*924_*926delinsCTA
XM_011520658.1:c.654-434_654-432delinsCTA	XP_011518960.1:n.654-434_654-432delinsCTA
XM_011520659.1:c.*900_*902delinsCTA	XP_011518961.1:n.*900_*902delinsCTA
XM_011520660.1:c.*895_*897delinsCTA	XP_011518962.1:n.*895_*897delinsCTA
XM_011520661.1:c.*10-434_*10-432delinsCTA	XP_011518963.1:n.*10-434_*10-432delinsCTA
XM_011520662.1:c.*931_*933delinsCTA	XP_011518964.1:n.*931_*933delinsCTA
XM_011520663.1:c.526-434_526-432delinsCTA	XP_011518965.1:n.526-434_526-432delinsCTA
XM_011520664.1:c.526-521_526-519delinsCTA	XP_011518966.1:n.526-521_526-519delinsCTA
XR_242889.3:n.956-434_956-432delinsCTA
XR_931290.1:n.1877_1879delinsCTA
NM_001129998.2:c.681-434_681-432delinsCTA	NP_001123470.1:n.681-434_681-432delinsCTA
NM_001319241.1:c.372-434_372-432delinsCTA	NP_001306170.1:n.372-434_372-432delinsCTA
NM_001319242.1:c.*2151_*2153delinsCTA	NP_001306171.1:n.*2151_*2153delinsCTA
NM_205852.3:c.*2151_*2153delinsCTA	NP_995324.2:n.*2151_*2153delinsCTA
NR_135049.1:n.961-434_961-432delinsCTA
XM_011520658.2:c.654-434_654-432delinsCTA	XP_011518960.1:n.654-434_654-432delinsCTA
XM_011520663.2:c.526-434_526-432delinsCTA	XP_011518965.1:n.526-434_526-432delinsCTA
XM_017019295.1:c.372-434_372-432delinsCTA	XP_016874784.1:n.372-434_372-432delinsCTA
XM_024448976.1:c.681-521_681-519delinsCTA	XP_024304744.1:n.681-521_681-519delinsCTA
XM_024448977.1:c.*2158_*2160delinsCTA	XP_024304745.1:n.*2158_*2160delinsCTA
XR_002957401.1:n.106-1751_106-1749delinsTAG
NM_001129998.3:c.681-434_681-432delinsCTA MANE Select	NP_001123470.1:n.681-434_681-432delinsCTA
NM_001387138.1:c.681-521_681-519delinsCTA	NP_001374067.1:n.681-521_681-519delinsCTA
NR_169587.1:n.258-1751_258-1749delinsTAG