Canonical Allele Identifier: CA2015799033

Gene: CLEC7A

Linked Data

• dbSNP Id: rs1948201986

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.10124333_10124334insATGGAAC , CM000674.2:g.10124333_10124334insATGGAAC	GRCh38
NC_000012.11:g.10276932_10276933insATGGAAC , CM000674.1:g.10276932_10276933insATGGAAC	GRCh37
NC_000012.10:g.10168199_10168200insATGGAAC	NCBI36
NG_016291.1:g.10936_10937insGTTCCAT , LRG_179:g.10936_10937insGTTCCAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000304084.13:c.492+963_492+964insGTTCCAT MANE Select	ENSP00000302569.8:n.492+963_492+964insGTTCCAT
ENST00000298523.9:c.354+963_354+964insGTTCCAT	ENSP00000298523.5:n.354+963_354+964insGTTCCAT
ENST00000304084.12:c.492+963_492+964insGTTCCAT	ENSP00000302569.8:n.492+963_492+964insGTTCCAT
ENST00000349926.9:c.104-971_104-970insGTTCCAT	ENSP00000344723.5:n.104-971_104-970insGTTCCAT
ENST00000353231.9:c.354+963_354+964insGTTCCAT	ENSP00000266456.6:n.354+963_354+964insGTTCCAT
ENST00000396484.6:c.255+963_255+964insGTTCCAT	ENSP00000379743.2:n.255+963_255+964insGTTCCAT
ENST00000465100.5:c.629+753_629+754insGTTCCAT	ENSP00000436923.1:n.629+753_629+754insGTTCCAT
ENST00000529761.5:c.492+963_492+964insGTTCCAT	ENSP00000432876.1:n.492+963_492+964insGTTCCAT
ENST00000531192.5:c.579+753_579+754insGTTCCAT	ENSP00000434392.1:n.579+753_579+754insGTTCCAT
ENST00000533022.5:c.492+963_492+964insGTTCCAT	ENSP00000431461.1:n.492+963_492+964insGTTCCAT
ENST00000534609.5:n.1792+753_1792+754insGTTCCAT
NM_022570.4:c.354+963_354+964insGTTCCAT	NP_072092.2:n.354+963_354+964insGTTCCAT
NM_197947.2:c.492+963_492+964insGTTCCAT , LRG_179t1:c.492+963_492+964insGTTCCAT	NP_922938.1:n.492+963_492+964insGTTCCAT
NM_197948.2:c.492+963_492+964insGTTCCAT	NP_922939.1:n.492+963_492+964insGTTCCAT
NM_197949.2:c.354+963_354+964insGTTCCAT	NP_922940.1:n.354+963_354+964insGTTCCAT
NM_197950.2:c.255+963_255+964insGTTCCAT	NP_922941.1:n.255+963_255+964insGTTCCAT
NR_125336.1:n.766+753_766+754insGTTCCAT
XM_005253467.3:c.492+963_492+964insGTTCCAT	XP_005253524.1:n.492+963_492+964insGTTCCAT
XM_006719135.2:c.579+753_579+754insGTTCCAT	XP_006719198.1:n.579+753_579+754insGTTCCAT
XR_931351.1:n.159-6748_159-6747insATGGAAC
XR_931352.1:n.159-6748_159-6747insATGGAAC
XM_006719135.3:c.579+753_579+754insGTTCCAT	XP_006719198.1:n.579+753_579+754insGTTCCAT
XM_017019822.1:c.575+757_575+758insGTTCCAT	XP_016875311.1:n.575+757_575+758insGTTCCAT
XM_017019823.1:c.437+757_437+758insGTTCCAT	XP_016875312.1:n.437+757_437+758insGTTCCAT
XM_024449132.1:c.575+757_575+758insGTTCCAT	XP_024304900.1:n.575+757_575+758insGTTCCAT
XM_024449133.1:c.441+753_441+754insGTTCCAT	XP_024304901.1:n.441+753_441+754insGTTCCAT
XR_931351.2:n.160-6748_160-6747insATGGAAC
XR_931352.2:n.160-6748_160-6747insATGGAAC
NM_022570.5:c.354+963_354+964insGTTCCAT	NP_072092.2:n.354+963_354+964insGTTCCAT
NM_197947.3:c.492+963_492+964insGTTCCAT MANE Select	NP_922938.1:n.492+963_492+964insGTTCCAT
NM_197948.3:c.492+963_492+964insGTTCCAT	NP_922939.1:n.492+963_492+964insGTTCCAT
NM_197949.3:c.354+963_354+964insGTTCCAT	NP_922940.1:n.354+963_354+964insGTTCCAT
NM_197950.3:c.255+963_255+964insGTTCCAT	NP_922941.1:n.255+963_255+964insGTTCCAT
NR_125336.2:n.696+753_696+754insGTTCCAT