Canonical Allele Identifier: CA2015750710

Gene: CLEC12B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.10017719T= , CM000674.2:g.10017719T=	GRCh38
NC_000012.11:g.10170318T= , CM000674.1:g.10170318T=	GRCh37
NC_000012.10:g.10061585T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338896.11:c.681-612T= MANE Select	ENSP00000344563.5:n.681-612T=
ENST00000338896.10:c.681-612T=	ENSP00000344563.5:n.681-612T=
ENST00000338896.9:c.681-612T=	ENSP00000344563.5:n.681-612T=
ENST00000396502.5:c.*1973T=	ENSP00000379759.1:n.*1973T=
ENST00000539155.1:c.*2466T=	ENSP00000444909.1:n.*2466T=
ENST00000544853.5:c.*129-612T=	ENSP00000439561.1:n.*129-612T=
NM_001129998.1:c.681-612T=	NP_001123470.1:n.681-612T=
NM_205852.2:c.*1973T=	NP_995324.2:n.*1973T=
NR_120484.1:n.249-1946A=
XM_006719070.2:c.681-699T=	XP_006719133.1:n.681-699T=
XM_006719071.2:c.*3-612T=	XP_006719134.1:n.*3-612T=
XM_006719072.1:c.*746T=	XP_006719135.1:n.*746T=
XM_011520658.1:c.654-612T=	XP_011518960.1:n.654-612T=
XM_011520659.1:c.*722T=	XP_011518961.1:n.*722T=
XM_011520660.1:c.*717T=	XP_011518962.1:n.*717T=
XM_011520661.1:c.*10-612T=	XP_011518963.1:n.*10-612T=
XM_011520662.1:c.*753T=	XP_011518964.1:n.*753T=
XM_011520663.1:c.526-612T=	XP_011518965.1:n.526-612T=
XM_011520664.1:c.526-699T=	XP_011518966.1:n.526-699T=
XR_242889.3:n.956-612T=
XR_931290.1:n.1699T=
NM_001129998.2:c.681-612T=	NP_001123470.1:n.681-612T=
NM_001319241.1:c.372-612T=	NP_001306170.1:n.372-612T=
NM_001319242.1:c.*1973T=	NP_001306171.1:n.*1973T=
NM_205852.3:c.*1973T=	NP_995324.2:n.*1973T=
NR_135049.1:n.961-612T=
XM_011520658.2:c.654-612T=	XP_011518960.1:n.654-612T=
XM_011520663.2:c.526-612T=	XP_011518965.1:n.526-612T=
XM_017019295.1:c.372-612T=	XP_016874784.1:n.372-612T=
XM_024448976.1:c.681-699T=	XP_024304744.1:n.681-699T=
XM_024448977.1:c.*1980T=	XP_024304745.1:n.*1980T=
XR_002957401.1:n.106-1571A=
NM_001129998.3:c.681-612T= MANE Select	NP_001123470.1:n.681-612T=
NM_001387138.1:c.681-699T=	NP_001374067.1:n.681-699T=
NR_169587.1:n.258-1571A=