Canonical Allele Identifier: CA2015750639

Gene: CLEC12B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.10017533C= , CM000674.2:g.10017533C=	GRCh38
NC_000012.11:g.10170132C= , CM000674.1:g.10170132C=	GRCh37
NC_000012.10:g.10061399C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338896.11:c.681-798C= MANE Select	ENSP00000344563.5:n.681-798C=
ENST00000338896.10:c.681-798C=	ENSP00000344563.5:n.681-798C=
ENST00000338896.9:c.681-798C=	ENSP00000344563.5:n.681-798C=
ENST00000396502.5:c.*1787C=	ENSP00000379759.1:n.*1787C=
ENST00000539155.1:c.*2280C=	ENSP00000444909.1:n.*2280C=
ENST00000544853.5:c.*129-798C=	ENSP00000439561.1:n.*129-798C=
NM_001129998.1:c.681-798C=	NP_001123470.1:n.681-798C=
NM_205852.2:c.*1787C=	NP_995324.2:n.*1787C=
NR_120484.1:n.249-1760G=
XM_006719070.2:c.681-885C=	XP_006719133.1:n.681-885C=
XM_006719071.2:c.*3-798C=	XP_006719134.1:n.*3-798C=
XM_006719072.1:c.*560C=	XP_006719135.1:n.*560C=
XM_011520658.1:c.654-798C=	XP_011518960.1:n.654-798C=
XM_011520659.1:c.*536C=	XP_011518961.1:n.*536C=
XM_011520660.1:c.*531C=	XP_011518962.1:n.*531C=
XM_011520661.1:c.*10-798C=	XP_011518963.1:n.*10-798C=
XM_011520662.1:c.*567C=	XP_011518964.1:n.*567C=
XM_011520663.1:c.526-798C=	XP_011518965.1:n.526-798C=
XM_011520664.1:c.526-885C=	XP_011518966.1:n.526-885C=
XR_242889.3:n.956-798C=
XR_931290.1:n.1513C=
NM_001129998.2:c.681-798C=	NP_001123470.1:n.681-798C=
NM_001319241.1:c.372-798C=	NP_001306170.1:n.372-798C=
NM_001319242.1:c.*1787C=	NP_001306171.1:n.*1787C=
NM_205852.3:c.*1787C=	NP_995324.2:n.*1787C=
NR_135049.1:n.961-798C=
XM_011520658.2:c.654-798C=	XP_011518960.1:n.654-798C=
XM_011520663.2:c.526-798C=	XP_011518965.1:n.526-798C=
XM_017019295.1:c.372-798C=	XP_016874784.1:n.372-798C=
XM_024448976.1:c.681-885C=	XP_024304744.1:n.681-885C=
XM_024448977.1:c.*1794C=	XP_024304745.1:n.*1794C=
XR_002957401.1:n.106-1385G=
NM_001129998.3:c.681-798C= MANE Select	NP_001123470.1:n.681-798C=
NM_001387138.1:c.681-885C=	NP_001374067.1:n.681-885C=
NR_169587.1:n.258-1385G=