Canonical Allele Identifier: CA2015798972
Gene: CLEC7A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.10124178T= , CM000674.2:g.10124178T= GRCh38
NC_000012.11:g.10276777T= , CM000674.1:g.10276777T= GRCh37
NC_000012.10:g.10168044T= NCBI36
NG_016291.1:g.11092A= , LRG_179:g.11092A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000304084.13:c.493-815A= MANE Select ENSP00000302569.8:n.493-815A=
ENST00000298523.9:c.354+1119A= ENSP00000298523.5:n.354+1119A=
ENST00000304084.12:c.493-815A= ENSP00000302569.8:n.493-815A=
ENST00000349926.9:c.104-815A= ENSP00000344723.5:n.104-815A=
ENST00000353231.9:c.355-815A= ENSP00000266456.6:n.355-815A=
ENST00000396484.6:c.256-815A= ENSP00000379743.2:n.256-815A=
ENST00000465100.5:c.630-815A= ENSP00000436923.1:n.630-815A=
ENST00000529761.5:c.493-815A= ENSP00000432876.1:n.493-815A=
ENST00000531192.5:c.*1-815A= ENSP00000434392.1:n.*1-815A=
ENST00000533022.5:c.492+1119A= ENSP00000431461.1:n.492+1119A=
ENST00000534609.5:n.1793-815A=
NM_022570.4:c.355-815A= NP_072092.2:n.355-815A=
NM_197947.2:c.493-815A= , LRG_179t1:c.493-815A= NP_922938.1:n.493-815A=
NM_197948.2:c.492+1119A= NP_922939.1:n.492+1119A=
NM_197949.2:c.354+1119A= NP_922940.1:n.354+1119A=
NM_197950.2:c.256-815A= NP_922941.1:n.256-815A=
NR_125336.1:n.767-815A=
XM_005253467.3:c.493-815A= XP_005253524.1:n.493-815A=
XM_006719135.2:c.579+909A= XP_006719198.1:n.579+909A=
XR_931351.1:n.159-6903T=
XR_931352.1:n.159-6903T=
XM_006719135.3:c.579+909A= XP_006719198.1:n.579+909A=
XM_017019822.1:c.575+913A= XP_016875311.1:n.575+913A=
XM_017019823.1:c.437+913A= XP_016875312.1:n.437+913A=
XM_024449132.1:c.576-815A= XP_024304900.1:n.576-815A=
XM_024449133.1:c.*1-815A= XP_024304901.1:n.*1-815A=
XR_931351.2:n.160-6903T=
XR_931352.2:n.160-6903T=
NM_022570.5:c.355-815A= NP_072092.2:n.355-815A=
NM_197947.3:c.493-815A= MANE Select NP_922938.1:n.493-815A=
NM_197948.3:c.492+1119A= NP_922939.1:n.492+1119A=
NM_197949.3:c.354+1119A= NP_922940.1:n.354+1119A=
NM_197950.3:c.256-815A= NP_922941.1:n.256-815A=
NR_125336.2:n.697-815A=