Canonical Allele Identifier: CA682687116

Gene: CLEC7A

Linked Data

• dbSNP Id: rs1486716075
• gnomAD v3: 12-10124347-A-G
• gnomAD v4: 12-10124347-A-G
• MyVariant Identifiers: chr12:g.10276946A>G (hg19) ; chr12:g.10124347A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.10124347A>G , CM000674.2:g.10124347A>G	GRCh38
NC_000012.11:g.10276946A>G , CM000674.1:g.10276946A>G	GRCh37
NC_000012.10:g.10168213A>G	NCBI36
NG_016291.1:g.10923T>C , LRG_179:g.10923T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304084.13:c.492+950T>C MANE Select	ENSP00000302569.8:n.492+950T>C
ENST00000298523.9:c.354+950T>C	ENSP00000298523.5:n.354+950T>C
ENST00000304084.12:c.492+950T>C	ENSP00000302569.8:n.492+950T>C
ENST00000349926.9:c.104-984T>C	ENSP00000344723.5:n.104-984T>C
ENST00000353231.9:c.354+950T>C	ENSP00000266456.6:n.354+950T>C
ENST00000396484.6:c.255+950T>C	ENSP00000379743.2:n.255+950T>C
ENST00000465100.5:c.629+740T>C	ENSP00000436923.1:n.629+740T>C
ENST00000529761.5:c.492+950T>C	ENSP00000432876.1:n.492+950T>C
ENST00000531192.5:c.579+740T>C	ENSP00000434392.1:n.579+740T>C
ENST00000533022.5:c.492+950T>C	ENSP00000431461.1:n.492+950T>C
ENST00000534609.5:n.1792+740T>C
NM_022570.4:c.354+950T>C	NP_072092.2:n.354+950T>C
NM_197947.2:c.492+950T>C , LRG_179t1:c.492+950T>C	NP_922938.1:n.492+950T>C
NM_197948.2:c.492+950T>C	NP_922939.1:n.492+950T>C
NM_197949.2:c.354+950T>C	NP_922940.1:n.354+950T>C
NM_197950.2:c.255+950T>C	NP_922941.1:n.255+950T>C
NR_125336.1:n.766+740T>C
XM_005253467.3:c.492+950T>C	XP_005253524.1:n.492+950T>C
XM_006719135.2:c.579+740T>C	XP_006719198.1:n.579+740T>C
XR_931351.1:n.159-6734A>G
XR_931352.1:n.159-6734A>G
XM_006719135.3:c.579+740T>C	XP_006719198.1:n.579+740T>C
XM_017019822.1:c.575+744T>C	XP_016875311.1:n.575+744T>C
XM_017019823.1:c.437+744T>C	XP_016875312.1:n.437+744T>C
XM_024449132.1:c.575+744T>C	XP_024304900.1:n.575+744T>C
XM_024449133.1:c.441+740T>C	XP_024304901.1:n.441+740T>C
XR_931351.2:n.160-6734A>G
XR_931352.2:n.160-6734A>G
NM_022570.5:c.354+950T>C	NP_072092.2:n.354+950T>C
NM_197947.3:c.492+950T>C MANE Select	NP_922938.1:n.492+950T>C
NM_197948.3:c.492+950T>C	NP_922939.1:n.492+950T>C
NM_197949.3:c.354+950T>C	NP_922940.1:n.354+950T>C
NM_197950.3:c.255+950T>C	NP_922941.1:n.255+950T>C
NR_125336.2:n.696+740T>C