Canonical Allele Identifier: CA2617597860

Gene: CLEC12B

Linked Data

• gnomAD v4: 12-10018042-GGAATTACATATTTATGAAGGAAATACAAATTCTCAGTCCAGGATTTAAGTATTTCTCTTAAA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.10018048_10018109del , CM000674.2:g.10018048_10018109del	GRCh38
NC_000012.11:g.10170647_10170708del , CM000674.1:g.10170647_10170708del	GRCh37
NC_000012.10:g.10061914_10061975del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338896.11:c.681-283_681-222del MANE Select	ENSP00000344563.5:n.681-283_681-222del
ENST00000338896.10:c.681-283_681-222del	ENSP00000344563.5:n.681-283_681-222del
ENST00000338896.9:c.681-283_681-222del	ENSP00000344563.5:n.681-283_681-222del
ENST00000544853.5:c.*129-283_*129-222del	ENSP00000439561.1:n.*129-283_*129-222del
NM_001129998.1:c.681-283_681-222del	NP_001123470.1:n.681-283_681-222del
NR_120484.1:n.249-2331_249-2270del
XM_006719070.2:c.681-370_681-309del	XP_006719133.1:n.681-370_681-309del
XM_006719071.2:c.*3-283_*3-222del	XP_006719134.1:n.*3-283_*3-222del
XM_011520658.1:c.654-283_654-222del	XP_011518960.1:n.654-283_654-222del
XM_011520661.1:c.*10-283_*10-222del	XP_011518963.1:n.*10-283_*10-222del
XM_011520663.1:c.526-283_526-222del	XP_011518965.1:n.526-283_526-222del
XM_011520664.1:c.526-370_526-309del	XP_011518966.1:n.526-370_526-309del
XR_242889.3:n.956-283_956-222del
NM_001129998.2:c.681-283_681-222del	NP_001123470.1:n.681-283_681-222del
NM_001319241.1:c.372-283_372-222del	NP_001306170.1:n.372-283_372-222del
NR_135049.1:n.961-283_961-222del
XM_011520658.2:c.654-283_654-222del	XP_011518960.1:n.654-283_654-222del
XM_011520663.2:c.526-283_526-222del	XP_011518965.1:n.526-283_526-222del
XM_017019295.1:c.372-283_372-222del	XP_016874784.1:n.372-283_372-222del
XM_024448976.1:c.681-370_681-309del	XP_024304744.1:n.681-370_681-309del
XR_002957401.1:n.106-1956_106-1895del
NM_001129998.3:c.681-283_681-222del MANE Select	NP_001123470.1:n.681-283_681-222del
NM_001387138.1:c.681-370_681-309del	NP_001374067.1:n.681-370_681-309del
NR_169587.1:n.258-1956_258-1895del