Canonical Allele Identifier: CA2015798982

Gene: CLEC7A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.10124197_10124201delinsCAGAT , CM000674.2:g.10124197_10124201delinsCAGAT	GRCh38
NC_000012.11:g.10276796_10276800delinsCAGAT , CM000674.1:g.10276796_10276800delinsCAGAT	GRCh37
NC_000012.10:g.10168063_10168067delinsCAGAT	NCBI36
NG_016291.1:g.11069_11073delinsATCTG , LRG_179:g.11069_11073delinsATCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304084.13:c.493-838_493-834delinsATCTG MANE Select	ENSP00000302569.8:n.493-838_493-834delinsATCTG
ENST00000298523.9:c.354+1096_354+1100delinsATCTG	ENSP00000298523.5:n.354+1096_354+1100delinsATCTG
ENST00000304084.12:c.493-838_493-834delinsATCTG	ENSP00000302569.8:n.493-838_493-834delinsATCTG
ENST00000349926.9:c.104-838_104-834delinsATCTG	ENSP00000344723.5:n.104-838_104-834delinsATCTG
ENST00000353231.9:c.355-838_355-834delinsATCTG	ENSP00000266456.6:n.355-838_355-834delinsATCTG
ENST00000396484.6:c.256-838_256-834delinsATCTG	ENSP00000379743.2:n.256-838_256-834delinsATCTG
ENST00000465100.5:c.630-838_630-834delinsATCTG	ENSP00000436923.1:n.630-838_630-834delinsATCTG
ENST00000529761.5:c.493-838_493-834delinsATCTG	ENSP00000432876.1:n.493-838_493-834delinsATCTG
ENST00000531192.5:c.*1-838_*1-834delinsATCTG	ENSP00000434392.1:n.*1-838_*1-834delinsATCTG
ENST00000533022.5:c.492+1096_492+1100delinsATCTG	ENSP00000431461.1:n.492+1096_492+1100delinsATCTG
ENST00000534609.5:n.1793-838_1793-834delinsATCTG
NM_022570.4:c.355-838_355-834delinsATCTG	NP_072092.2:n.355-838_355-834delinsATCTG
NM_197947.2:c.493-838_493-834delinsATCTG , LRG_179t1:c.493-838_493-834delinsATCTG	NP_922938.1:n.493-838_493-834delinsATCTG
NM_197948.2:c.492+1096_492+1100delinsATCTG	NP_922939.1:n.492+1096_492+1100delinsATCTG
NM_197949.2:c.354+1096_354+1100delinsATCTG	NP_922940.1:n.354+1096_354+1100delinsATCTG
NM_197950.2:c.256-838_256-834delinsATCTG	NP_922941.1:n.256-838_256-834delinsATCTG
NR_125336.1:n.767-838_767-834delinsATCTG
XM_005253467.3:c.493-838_493-834delinsATCTG	XP_005253524.1:n.493-838_493-834delinsATCTG
XM_006719135.2:c.579+886_579+890delinsATCTG	XP_006719198.1:n.579+886_579+890delinsATCTG
XR_931351.1:n.159-6884_159-6880delinsCAGAT
XR_931352.1:n.159-6884_159-6880delinsCAGAT
XM_006719135.3:c.579+886_579+890delinsATCTG	XP_006719198.1:n.579+886_579+890delinsATCTG
XM_017019822.1:c.575+890_575+894delinsATCTG	XP_016875311.1:n.575+890_575+894delinsATCTG
XM_017019823.1:c.437+890_437+894delinsATCTG	XP_016875312.1:n.437+890_437+894delinsATCTG
XM_024449132.1:c.576-838_576-834delinsATCTG	XP_024304900.1:n.576-838_576-834delinsATCTG
XM_024449133.1:c.*1-838_*1-834delinsATCTG	XP_024304901.1:n.*1-838_*1-834delinsATCTG
XR_931351.2:n.160-6884_160-6880delinsCAGAT
XR_931352.2:n.160-6884_160-6880delinsCAGAT
NM_022570.5:c.355-838_355-834delinsATCTG	NP_072092.2:n.355-838_355-834delinsATCTG
NM_197947.3:c.493-838_493-834delinsATCTG MANE Select	NP_922938.1:n.493-838_493-834delinsATCTG
NM_197948.3:c.492+1096_492+1100delinsATCTG	NP_922939.1:n.492+1096_492+1100delinsATCTG
NM_197949.3:c.354+1096_354+1100delinsATCTG	NP_922940.1:n.354+1096_354+1100delinsATCTG
NM_197950.3:c.256-838_256-834delinsATCTG	NP_922941.1:n.256-838_256-834delinsATCTG
NR_125336.2:n.697-838_697-834delinsATCTG