Canonical Allele Identifier: CA232780509

Gene: CLEC12B

Linked Data

• dbSNP Id: rs929656780
• gnomAD v2: 12-10170459-C-CT
• gnomAD v3: 12-10017860-C-CT
• gnomAD v4: 12-10017860-C-CT
• MyVariant Identifiers: chr12:g.10170459_10170460insT (hg19) ; chr12:g.10017860_10017861insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.10017861dup , CM000674.2:g.10017861dup	GRCh38
NC_000012.11:g.10170460dup , CM000674.1:g.10170460dup	GRCh37
NC_000012.10:g.10061727dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338896.11:c.681-470dup MANE Select	ENSP00000344563.5:n.681-470dup
ENST00000338896.10:c.681-470dup	ENSP00000344563.5:n.681-470dup
ENST00000338896.9:c.681-470dup	ENSP00000344563.5:n.681-470dup
ENST00000396502.5:c.*2115dup	ENSP00000379759.1:n.*2115dup
ENST00000539155.1:c.*2608dup	ENSP00000444909.1:n.*2608dup
ENST00000544853.5:c.*129-470dup	ENSP00000439561.1:n.*129-470dup
NM_001129998.1:c.681-470dup	NP_001123470.1:n.681-470dup
NM_205852.2:c.*2115dup	NP_995324.2:n.*2115dup
NR_120484.1:n.249-2088dup
XM_006719070.2:c.681-557dup	XP_006719133.1:n.681-557dup
XM_006719071.2:c.*3-470dup	XP_006719134.1:n.*3-470dup
XM_006719072.1:c.*888dup	XP_006719135.1:n.*888dup
XM_011520658.1:c.654-470dup	XP_011518960.1:n.654-470dup
XM_011520659.1:c.*864dup	XP_011518961.1:n.*864dup
XM_011520660.1:c.*859dup	XP_011518962.1:n.*859dup
XM_011520661.1:c.*10-470dup	XP_011518963.1:n.*10-470dup
XM_011520662.1:c.*895dup	XP_011518964.1:n.*895dup
XM_011520663.1:c.526-470dup	XP_011518965.1:n.526-470dup
XM_011520664.1:c.526-557dup	XP_011518966.1:n.526-557dup
XR_242889.3:n.956-470dup
XR_931290.1:n.1841dup
NM_001129998.2:c.681-470dup	NP_001123470.1:n.681-470dup
NM_001319241.1:c.372-470dup	NP_001306170.1:n.372-470dup
NM_001319242.1:c.*2115dup	NP_001306171.1:n.*2115dup
NM_205852.3:c.*2115dup	NP_995324.2:n.*2115dup
NR_135049.1:n.961-470dup
XM_011520658.2:c.654-470dup	XP_011518960.1:n.654-470dup
XM_011520663.2:c.526-470dup	XP_011518965.1:n.526-470dup
XM_017019295.1:c.372-470dup	XP_016874784.1:n.372-470dup
XM_024448976.1:c.681-557dup	XP_024304744.1:n.681-557dup
XM_024448977.1:c.*2122dup	XP_024304745.1:n.*2122dup
XR_002957401.1:n.106-1713dup
NM_001129998.3:c.681-470dup MANE Select	NP_001123470.1:n.681-470dup
NM_001387138.1:c.681-557dup	NP_001374067.1:n.681-557dup
NR_169587.1:n.258-1713dup