Canonical Allele Identifier: CA2015750748

Gene: CLEC12B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.10017815T= , CM000674.2:g.10017815T=	GRCh38
NC_000012.11:g.10170414T= , CM000674.1:g.10170414T=	GRCh37
NC_000012.10:g.10061681T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338896.11:c.681-516T= MANE Select	ENSP00000344563.5:n.681-516T=
ENST00000338896.10:c.681-516T=	ENSP00000344563.5:n.681-516T=
ENST00000338896.9:c.681-516T=	ENSP00000344563.5:n.681-516T=
ENST00000396502.5:c.*2069T=	ENSP00000379759.1:n.*2069T=
ENST00000539155.1:c.*2562T=	ENSP00000444909.1:n.*2562T=
ENST00000544853.5:c.*129-516T=	ENSP00000439561.1:n.*129-516T=
NM_001129998.1:c.681-516T=	NP_001123470.1:n.681-516T=
NM_205852.2:c.*2069T=	NP_995324.2:n.*2069T=
NR_120484.1:n.249-2042A=
XM_006719070.2:c.681-603T=	XP_006719133.1:n.681-603T=
XM_006719071.2:c.*3-516T=	XP_006719134.1:n.*3-516T=
XM_006719072.1:c.*842T=	XP_006719135.1:n.*842T=
XM_011520658.1:c.654-516T=	XP_011518960.1:n.654-516T=
XM_011520659.1:c.*818T=	XP_011518961.1:n.*818T=
XM_011520660.1:c.*813T=	XP_011518962.1:n.*813T=
XM_011520661.1:c.*10-516T=	XP_011518963.1:n.*10-516T=
XM_011520662.1:c.*849T=	XP_011518964.1:n.*849T=
XM_011520663.1:c.526-516T=	XP_011518965.1:n.526-516T=
XM_011520664.1:c.526-603T=	XP_011518966.1:n.526-603T=
XR_242889.3:n.956-516T=
XR_931290.1:n.1795T=
NM_001129998.2:c.681-516T=	NP_001123470.1:n.681-516T=
NM_001319241.1:c.372-516T=	NP_001306170.1:n.372-516T=
NM_001319242.1:c.*2069T=	NP_001306171.1:n.*2069T=
NM_205852.3:c.*2069T=	NP_995324.2:n.*2069T=
NR_135049.1:n.961-516T=
XM_011520658.2:c.654-516T=	XP_011518960.1:n.654-516T=
XM_011520663.2:c.526-516T=	XP_011518965.1:n.526-516T=
XM_017019295.1:c.372-516T=	XP_016874784.1:n.372-516T=
XM_024448976.1:c.681-603T=	XP_024304744.1:n.681-603T=
XM_024448977.1:c.*2076T=	XP_024304745.1:n.*2076T=
XR_002957401.1:n.106-1667A=
NM_001129998.3:c.681-516T= MANE Select	NP_001123470.1:n.681-516T=
NM_001387138.1:c.681-603T=	NP_001374067.1:n.681-603T=
NR_169587.1:n.258-1667A=