Canonical Allele Identifier: CA2015750716

Gene: CLEC12B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.10017736T= , CM000674.2:g.10017736T=	GRCh38
NC_000012.11:g.10170335T= , CM000674.1:g.10170335T=	GRCh37
NC_000012.10:g.10061602T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338896.11:c.681-595T= MANE Select	ENSP00000344563.5:n.681-595T=
ENST00000338896.10:c.681-595T=	ENSP00000344563.5:n.681-595T=
ENST00000338896.9:c.681-595T=	ENSP00000344563.5:n.681-595T=
ENST00000396502.5:c.*1990T=	ENSP00000379759.1:n.*1990T=
ENST00000539155.1:c.*2483T=	ENSP00000444909.1:n.*2483T=
ENST00000544853.5:c.*129-595T=	ENSP00000439561.1:n.*129-595T=
NM_001129998.1:c.681-595T=	NP_001123470.1:n.681-595T=
NM_205852.2:c.*1990T=	NP_995324.2:n.*1990T=
NR_120484.1:n.249-1963A=
XM_006719070.2:c.681-682T=	XP_006719133.1:n.681-682T=
XM_006719071.2:c.*3-595T=	XP_006719134.1:n.*3-595T=
XM_006719072.1:c.*763T=	XP_006719135.1:n.*763T=
XM_011520658.1:c.654-595T=	XP_011518960.1:n.654-595T=
XM_011520659.1:c.*739T=	XP_011518961.1:n.*739T=
XM_011520660.1:c.*734T=	XP_011518962.1:n.*734T=
XM_011520661.1:c.*10-595T=	XP_011518963.1:n.*10-595T=
XM_011520662.1:c.*770T=	XP_011518964.1:n.*770T=
XM_011520663.1:c.526-595T=	XP_011518965.1:n.526-595T=
XM_011520664.1:c.526-682T=	XP_011518966.1:n.526-682T=
XR_242889.3:n.956-595T=
XR_931290.1:n.1716T=
NM_001129998.2:c.681-595T=	NP_001123470.1:n.681-595T=
NM_001319241.1:c.372-595T=	NP_001306170.1:n.372-595T=
NM_001319242.1:c.*1990T=	NP_001306171.1:n.*1990T=
NM_205852.3:c.*1990T=	NP_995324.2:n.*1990T=
NR_135049.1:n.961-595T=
XM_011520658.2:c.654-595T=	XP_011518960.1:n.654-595T=
XM_011520663.2:c.526-595T=	XP_011518965.1:n.526-595T=
XM_017019295.1:c.372-595T=	XP_016874784.1:n.372-595T=
XM_024448976.1:c.681-682T=	XP_024304744.1:n.681-682T=
XM_024448977.1:c.*1997T=	XP_024304745.1:n.*1997T=
XR_002957401.1:n.106-1588A=
NM_001129998.3:c.681-595T= MANE Select	NP_001123470.1:n.681-595T=
NM_001387138.1:c.681-682T=	NP_001374067.1:n.681-682T=
NR_169587.1:n.258-1588A=