Canonical Allele Identifier: CA2617597745

Gene: CLEC12B

Linked Data

• gnomAD v4: 12-10017897-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.10017898dup , CM000674.2:g.10017898dup	GRCh38
NC_000012.11:g.10170497dup , CM000674.1:g.10170497dup	GRCh37
NC_000012.10:g.10061764dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338896.11:c.681-433dup MANE Select	ENSP00000344563.5:n.681-433dup
ENST00000338896.10:c.681-433dup	ENSP00000344563.5:n.681-433dup
ENST00000338896.9:c.681-433dup	ENSP00000344563.5:n.681-433dup
ENST00000396502.5:c.*2152dup	ENSP00000379759.1:n.*2152dup
ENST00000539155.1:c.*2645dup	ENSP00000444909.1:n.*2645dup
ENST00000544853.5:c.*129-433dup	ENSP00000439561.1:n.*129-433dup
NM_001129998.1:c.681-433dup	NP_001123470.1:n.681-433dup
NM_205852.2:c.*2152dup	NP_995324.2:n.*2152dup
NR_120484.1:n.249-2125dup
XM_006719070.2:c.681-520dup	XP_006719133.1:n.681-520dup
XM_006719071.2:c.*3-433dup	XP_006719134.1:n.*3-433dup
XM_006719072.1:c.*925dup	XP_006719135.1:n.*925dup
XM_011520658.1:c.654-433dup	XP_011518960.1:n.654-433dup
XM_011520659.1:c.*901dup	XP_011518961.1:n.*901dup
XM_011520660.1:c.*896dup	XP_011518962.1:n.*896dup
XM_011520661.1:c.*10-433dup	XP_011518963.1:n.*10-433dup
XM_011520662.1:c.*932dup	XP_011518964.1:n.*932dup
XM_011520663.1:c.526-433dup	XP_011518965.1:n.526-433dup
XM_011520664.1:c.526-520dup	XP_011518966.1:n.526-520dup
XR_242889.3:n.956-433dup
XR_931290.1:n.1878dup
NM_001129998.2:c.681-433dup	NP_001123470.1:n.681-433dup
NM_001319241.1:c.372-433dup	NP_001306170.1:n.372-433dup
NM_001319242.1:c.*2152dup	NP_001306171.1:n.*2152dup
NM_205852.3:c.*2152dup	NP_995324.2:n.*2152dup
NR_135049.1:n.961-433dup
XM_011520658.2:c.654-433dup	XP_011518960.1:n.654-433dup
XM_011520663.2:c.526-433dup	XP_011518965.1:n.526-433dup
XM_017019295.1:c.372-433dup	XP_016874784.1:n.372-433dup
XM_024448976.1:c.681-520dup	XP_024304744.1:n.681-520dup
XM_024448977.1:c.*2159dup	XP_024304745.1:n.*2159dup
XR_002957401.1:n.106-1750dup
NM_001129998.3:c.681-433dup MANE Select	NP_001123470.1:n.681-433dup
NM_001387138.1:c.681-520dup	NP_001374067.1:n.681-520dup
NR_169587.1:n.258-1750dup