Canonical Allele Identifier: CA2015750890

Gene: CLEC12B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.10018168_10018169delinsAT , CM000674.2:g.10018168_10018169delinsAT	GRCh38
NC_000012.11:g.10170767_10170768delinsAT , CM000674.1:g.10170767_10170768delinsAT	GRCh37
NC_000012.10:g.10062034_10062035delinsAT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338896.11:c.681-163_681-162delinsAT MANE Select	ENSP00000344563.5:n.681-163_681-162delinsAT
ENST00000338896.10:c.681-163_681-162delinsAT	ENSP00000344563.5:n.681-163_681-162delinsAT
ENST00000338896.9:c.681-163_681-162delinsAT	ENSP00000344563.5:n.681-163_681-162delinsAT
ENST00000544853.5:c.*129-163_*129-162delinsAT	ENSP00000439561.1:n.*129-163_*129-162delinsAT
NM_001129998.1:c.681-163_681-162delinsAT	NP_001123470.1:n.681-163_681-162delinsAT
NR_120484.1:n.249-2396_249-2395delinsAT
XM_006719070.2:c.681-250_681-249delinsAT	XP_006719133.1:n.681-250_681-249delinsAT
XM_006719071.2:c.*3-163_*3-162delinsAT	XP_006719134.1:n.*3-163_*3-162delinsAT
XM_011520658.1:c.654-163_654-162delinsAT	XP_011518960.1:n.654-163_654-162delinsAT
XM_011520661.1:c.*10-163_*10-162delinsAT	XP_011518963.1:n.*10-163_*10-162delinsAT
XM_011520663.1:c.526-163_526-162delinsAT	XP_011518965.1:n.526-163_526-162delinsAT
XM_011520664.1:c.526-250_526-249delinsAT	XP_011518966.1:n.526-250_526-249delinsAT
XR_242889.3:n.956-163_956-162delinsAT
NM_001129998.2:c.681-163_681-162delinsAT	NP_001123470.1:n.681-163_681-162delinsAT
NM_001319241.1:c.372-163_372-162delinsAT	NP_001306170.1:n.372-163_372-162delinsAT
NR_135049.1:n.961-163_961-162delinsAT
XM_011520658.2:c.654-163_654-162delinsAT	XP_011518960.1:n.654-163_654-162delinsAT
XM_011520663.2:c.526-163_526-162delinsAT	XP_011518965.1:n.526-163_526-162delinsAT
XM_017019295.1:c.372-163_372-162delinsAT	XP_016874784.1:n.372-163_372-162delinsAT
XM_024448976.1:c.681-250_681-249delinsAT	XP_024304744.1:n.681-250_681-249delinsAT
XR_002957401.1:n.106-2021_106-2020delinsAT
NM_001129998.3:c.681-163_681-162delinsAT MANE Select	NP_001123470.1:n.681-163_681-162delinsAT
NM_001387138.1:c.681-250_681-249delinsAT	NP_001374067.1:n.681-250_681-249delinsAT
NR_169587.1:n.258-2021_258-2020delinsAT