Canonical Allele Identifier: CA2575076773

Gene: CLEC12B

Linked Data

• gnomAD v4: 12-10017705-G-GA

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.10017712dup , CM000674.2:g.10017712dup	GRCh38
NC_000012.11:g.10170311dup , CM000674.1:g.10170311dup	GRCh37
NC_000012.10:g.10061578dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338896.11:c.681-619dup MANE Select	ENSP00000344563.5:n.681-619dup
ENST00000338896.10:c.681-619dup	ENSP00000344563.5:n.681-619dup
ENST00000338896.9:c.681-619dup	ENSP00000344563.5:n.681-619dup
ENST00000396502.5:c.*1966dup	ENSP00000379759.1:n.*1966dup
ENST00000539155.1:c.*2459dup	ENSP00000444909.1:n.*2459dup
ENST00000544853.5:c.*129-619dup	ENSP00000439561.1:n.*129-619dup
NM_001129998.1:c.681-619dup	NP_001123470.1:n.681-619dup
NM_205852.2:c.*1966dup	NP_995324.2:n.*1966dup
NR_120484.1:n.249-1933dup
XM_006719070.2:c.681-706dup	XP_006719133.1:n.681-706dup
XM_006719071.2:c.*3-619dup	XP_006719134.1:n.*3-619dup
XM_006719072.1:c.*739dup	XP_006719135.1:n.*739dup
XM_011520658.1:c.654-619dup	XP_011518960.1:n.654-619dup
XM_011520659.1:c.*715dup	XP_011518961.1:n.*715dup
XM_011520660.1:c.*710dup	XP_011518962.1:n.*710dup
XM_011520661.1:c.*10-619dup	XP_011518963.1:n.*10-619dup
XM_011520662.1:c.*746dup	XP_011518964.1:n.*746dup
XM_011520663.1:c.526-619dup	XP_011518965.1:n.526-619dup
XM_011520664.1:c.526-706dup	XP_011518966.1:n.526-706dup
XR_242889.3:n.956-619dup
XR_931290.1:n.1692dup
NM_001129998.2:c.681-619dup	NP_001123470.1:n.681-619dup
NM_001319241.1:c.372-619dup	NP_001306170.1:n.372-619dup
NM_001319242.1:c.*1966dup	NP_001306171.1:n.*1966dup
NM_205852.3:c.*1966dup	NP_995324.2:n.*1966dup
NR_135049.1:n.961-619dup
XM_011520658.2:c.654-619dup	XP_011518960.1:n.654-619dup
XM_011520663.2:c.526-619dup	XP_011518965.1:n.526-619dup
XM_017019295.1:c.372-619dup	XP_016874784.1:n.372-619dup
XM_024448976.1:c.681-706dup	XP_024304744.1:n.681-706dup
XM_024448977.1:c.*1973dup	XP_024304745.1:n.*1973dup
XR_002957401.1:n.106-1558dup
NM_001129998.3:c.681-619dup MANE Select	NP_001123470.1:n.681-619dup
NM_001387138.1:c.681-706dup	NP_001374067.1:n.681-706dup
NR_169587.1:n.258-1558dup