Canonical Allele Identifier: CA2015750791
Gene: CLEC12B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.10017896A= , CM000674.2:g.10017896A= GRCh38
NC_000012.11:g.10170495A= , CM000674.1:g.10170495A= GRCh37
NC_000012.10:g.10061762A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000338896.11:c.681-435A= MANE Select ENSP00000344563.5:n.681-435A=
ENST00000338896.10:c.681-435A= ENSP00000344563.5:n.681-435A=
ENST00000338896.9:c.681-435A= ENSP00000344563.5:n.681-435A=
ENST00000396502.5:c.*2150A= ENSP00000379759.1:n.*2150A=
ENST00000539155.1:c.*2643A= ENSP00000444909.1:n.*2643A=
ENST00000544853.5:c.*129-435A= ENSP00000439561.1:n.*129-435A=
NM_001129998.1:c.681-435A= NP_001123470.1:n.681-435A=
NM_205852.2:c.*2150A= NP_995324.2:n.*2150A=
NR_120484.1:n.249-2123T=
XM_006719070.2:c.681-522A= XP_006719133.1:n.681-522A=
XM_006719071.2:c.*3-435A= XP_006719134.1:n.*3-435A=
XM_006719072.1:c.*923A= XP_006719135.1:n.*923A=
XM_011520658.1:c.654-435A= XP_011518960.1:n.654-435A=
XM_011520659.1:c.*899A= XP_011518961.1:n.*899A=
XM_011520660.1:c.*894A= XP_011518962.1:n.*894A=
XM_011520661.1:c.*10-435A= XP_011518963.1:n.*10-435A=
XM_011520662.1:c.*930A= XP_011518964.1:n.*930A=
XM_011520663.1:c.526-435A= XP_011518965.1:n.526-435A=
XM_011520664.1:c.526-522A= XP_011518966.1:n.526-522A=
XR_242889.3:n.956-435A=
XR_931290.1:n.1876A=
NM_001129998.2:c.681-435A= NP_001123470.1:n.681-435A=
NM_001319241.1:c.372-435A= NP_001306170.1:n.372-435A=
NM_001319242.1:c.*2150A= NP_001306171.1:n.*2150A=
NM_205852.3:c.*2150A= NP_995324.2:n.*2150A=
NR_135049.1:n.961-435A=
XM_011520658.2:c.654-435A= XP_011518960.1:n.654-435A=
XM_011520663.2:c.526-435A= XP_011518965.1:n.526-435A=
XM_017019295.1:c.372-435A= XP_016874784.1:n.372-435A=
XM_024448976.1:c.681-522A= XP_024304744.1:n.681-522A=
XM_024448977.1:c.*2157A= XP_024304745.1:n.*2157A=
XR_002957401.1:n.106-1748T=
NM_001129998.3:c.681-435A= MANE Select NP_001123470.1:n.681-435A=
NM_001387138.1:c.681-522A= NP_001374067.1:n.681-522A=
NR_169587.1:n.258-1748T=