Canonical Allele Identifier: CA2015750895

Gene: CLEC12B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.10018181T= , CM000674.2:g.10018181T=	GRCh38
NC_000012.11:g.10170780T= , CM000674.1:g.10170780T=	GRCh37
NC_000012.10:g.10062047T=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000338896.11:c.681-150T= MANE Select	ENSP00000344563.5:n.681-150T=
ENST00000338896.10:c.681-150T=	ENSP00000344563.5:n.681-150T=
ENST00000338896.9:c.681-150T=	ENSP00000344563.5:n.681-150T=
ENST00000544853.5:c.*129-150T=	ENSP00000439561.1:n.*129-150T=
NM_001129998.1:c.681-150T=	NP_001123470.1:n.681-150T=
NR_120484.1:n.249-2408A=
XM_006719070.2:c.681-237T=	XP_006719133.1:n.681-237T=
XM_006719071.2:c.*3-150T=	XP_006719134.1:n.*3-150T=
XM_011520658.1:c.654-150T=	XP_011518960.1:n.654-150T=
XM_011520661.1:c.*10-150T=	XP_011518963.1:n.*10-150T=
XM_011520663.1:c.526-150T=	XP_011518965.1:n.526-150T=
XM_011520664.1:c.526-237T=	XP_011518966.1:n.526-237T=
XR_242889.3:n.956-150T=
NM_001129998.2:c.681-150T=	NP_001123470.1:n.681-150T=
NM_001319241.1:c.372-150T=	NP_001306170.1:n.372-150T=
NR_135049.1:n.961-150T=
XM_011520658.2:c.654-150T=	XP_011518960.1:n.654-150T=
XM_011520663.2:c.526-150T=	XP_011518965.1:n.526-150T=
XM_017019295.1:c.372-150T=	XP_016874784.1:n.372-150T=
XM_024448976.1:c.681-237T=	XP_024304744.1:n.681-237T=
XR_002957401.1:n.106-2033A=
NM_001129998.3:c.681-150T= MANE Select	NP_001123470.1:n.681-150T=
NM_001387138.1:c.681-237T=	NP_001374067.1:n.681-237T=
NR_169587.1:n.258-2033A=