Canonical Allele Identifier: CA2575076748

Gene: CLEC12B

Linked Data

• gnomAD v4: 12-10017473-TAATC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.10017476_10017479del , CM000674.2:g.10017476_10017479del	GRCh38
NC_000012.11:g.10170075_10170078del , CM000674.1:g.10170075_10170078del	GRCh37
NC_000012.10:g.10061342_10061345del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000338896.11:c.681-855_681-852del MANE Select	ENSP00000344563.5:n.681-855_681-852del
ENST00000338896.10:c.681-855_681-852del	ENSP00000344563.5:n.681-855_681-852del
ENST00000338896.9:c.681-855_681-852del	ENSP00000344563.5:n.681-855_681-852del
ENST00000396502.5:c.*1730_*1733del	ENSP00000379759.1:n.*1730_*1733del
ENST00000539155.1:c.*2223_*2226del	ENSP00000444909.1:n.*2223_*2226del
ENST00000544853.5:c.*129-855_*129-852del	ENSP00000439561.1:n.*129-855_*129-852del
NM_001129998.1:c.681-855_681-852del	NP_001123470.1:n.681-855_681-852del
NM_205852.2:c.*1730_*1733del	NP_995324.2:n.*1730_*1733del
NR_120484.1:n.249-1704_249-1701del
XM_006719070.2:c.681-942_681-939del	XP_006719133.1:n.681-942_681-939del
XM_006719071.2:c.*3-855_*3-852del	XP_006719134.1:n.*3-855_*3-852del
XM_006719072.1:c.*503_*506del	XP_006719135.1:n.*503_*506del
XM_011520658.1:c.654-855_654-852del	XP_011518960.1:n.654-855_654-852del
XM_011520659.1:c.*479_*482del	XP_011518961.1:n.*479_*482del
XM_011520660.1:c.*474_*477del	XP_011518962.1:n.*474_*477del
XM_011520661.1:c.*10-855_*10-852del	XP_011518963.1:n.*10-855_*10-852del
XM_011520662.1:c.*510_*513del	XP_011518964.1:n.*510_*513del
XM_011520663.1:c.526-855_526-852del	XP_011518965.1:n.526-855_526-852del
XM_011520664.1:c.526-942_526-939del	XP_011518966.1:n.526-942_526-939del
XR_242889.3:n.956-855_956-852del
XR_931290.1:n.1456_1459del
NM_001129998.2:c.681-855_681-852del	NP_001123470.1:n.681-855_681-852del
NM_001319241.1:c.372-855_372-852del	NP_001306170.1:n.372-855_372-852del
NM_001319242.1:c.*1730_*1733del	NP_001306171.1:n.*1730_*1733del
NM_205852.3:c.*1730_*1733del	NP_995324.2:n.*1730_*1733del
NR_135049.1:n.961-855_961-852del
XM_011520658.2:c.654-855_654-852del	XP_011518960.1:n.654-855_654-852del
XM_011520663.2:c.526-855_526-852del	XP_011518965.1:n.526-855_526-852del
XM_017019295.1:c.372-855_372-852del	XP_016874784.1:n.372-855_372-852del
XM_024448976.1:c.681-942_681-939del	XP_024304744.1:n.681-942_681-939del
XM_024448977.1:c.*1737_*1740del	XP_024304745.1:n.*1737_*1740del
XR_002957401.1:n.106-1329_106-1326del
NM_001129998.3:c.681-855_681-852del MANE Select	NP_001123470.1:n.681-855_681-852del
NM_001387138.1:c.681-942_681-939del	NP_001374067.1:n.681-942_681-939del
NR_169587.1:n.258-1329_258-1326del