Canonical Allele Identifier: CA2015750660

Gene: CLEC12B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.10017569A= , CM000674.2:g.10017569A=	GRCh38
NC_000012.11:g.10170168A= , CM000674.1:g.10170168A=	GRCh37
NC_000012.10:g.10061435A=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000338896.11:c.681-762A= MANE Select	ENSP00000344563.5:n.681-762A=
ENST00000338896.10:c.681-762A=	ENSP00000344563.5:n.681-762A=
ENST00000338896.9:c.681-762A=	ENSP00000344563.5:n.681-762A=
ENST00000396502.5:c.*1823A=	ENSP00000379759.1:n.*1823A=
ENST00000539155.1:c.*2316A=	ENSP00000444909.1:n.*2316A=
ENST00000544853.5:c.*129-762A=	ENSP00000439561.1:n.*129-762A=
NM_001129998.1:c.681-762A=	NP_001123470.1:n.681-762A=
NM_205852.2:c.*1823A=	NP_995324.2:n.*1823A=
NR_120484.1:n.249-1796T=
XM_006719070.2:c.681-849A=	XP_006719133.1:n.681-849A=
XM_006719071.2:c.*3-762A=	XP_006719134.1:n.*3-762A=
XM_006719072.1:c.*596A=	XP_006719135.1:n.*596A=
XM_011520658.1:c.654-762A=	XP_011518960.1:n.654-762A=
XM_011520659.1:c.*572A=	XP_011518961.1:n.*572A=
XM_011520660.1:c.*567A=	XP_011518962.1:n.*567A=
XM_011520661.1:c.*10-762A=	XP_011518963.1:n.*10-762A=
XM_011520662.1:c.*603A=	XP_011518964.1:n.*603A=
XM_011520663.1:c.526-762A=	XP_011518965.1:n.526-762A=
XM_011520664.1:c.526-849A=	XP_011518966.1:n.526-849A=
XR_242889.3:n.956-762A=
XR_931290.1:n.1549A=
NM_001129998.2:c.681-762A=	NP_001123470.1:n.681-762A=
NM_001319241.1:c.372-762A=	NP_001306170.1:n.372-762A=
NM_001319242.1:c.*1823A=	NP_001306171.1:n.*1823A=
NM_205852.3:c.*1823A=	NP_995324.2:n.*1823A=
NR_135049.1:n.961-762A=
XM_011520658.2:c.654-762A=	XP_011518960.1:n.654-762A=
XM_011520663.2:c.526-762A=	XP_011518965.1:n.526-762A=
XM_017019295.1:c.372-762A=	XP_016874784.1:n.372-762A=
XM_024448976.1:c.681-849A=	XP_024304744.1:n.681-849A=
XM_024448977.1:c.*1830A=	XP_024304745.1:n.*1830A=
XR_002957401.1:n.106-1421T=
NM_001129998.3:c.681-762A= MANE Select	NP_001123470.1:n.681-762A=
NM_001387138.1:c.681-849A=	NP_001374067.1:n.681-849A=
NR_169587.1:n.258-1421T=