Canonical Allele Identifier: CA232779852

Gene: CLEC7A

Linked Data

• dbSNP Id: rs892946613
• gnomAD v3: 12-10124274-G-A
• gnomAD v4: 12-10124274-G-A
• MyVariant Identifiers: chr12:g.10276873G>A (hg19) ; chr12:g.10124274G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.10124274G>A , CM000674.2:g.10124274G>A	GRCh38
NC_000012.11:g.10276873G>A , CM000674.1:g.10276873G>A	GRCh37
NC_000012.10:g.10168140G>A	NCBI36
NG_016291.1:g.10996C>T , LRG_179:g.10996C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000304084.13:c.493-911C>T MANE Select	ENSP00000302569.8:n.493-911C>T
ENST00000298523.9:c.354+1023C>T	ENSP00000298523.5:n.354+1023C>T
ENST00000304084.12:c.493-911C>T	ENSP00000302569.8:n.493-911C>T
ENST00000349926.9:c.104-911C>T	ENSP00000344723.5:n.104-911C>T
ENST00000353231.9:c.355-911C>T	ENSP00000266456.6:n.355-911C>T
ENST00000396484.6:c.256-911C>T	ENSP00000379743.2:n.256-911C>T
ENST00000465100.5:c.629+813C>T	ENSP00000436923.1:n.629+813C>T
ENST00000529761.5:c.493-911C>T	ENSP00000432876.1:n.493-911C>T
ENST00000531192.5:c.579+813C>T	ENSP00000434392.1:n.579+813C>T
ENST00000533022.5:c.492+1023C>T	ENSP00000431461.1:n.492+1023C>T
ENST00000534609.5:n.1792+813C>T
NM_022570.4:c.355-911C>T	NP_072092.2:n.355-911C>T
NM_197947.2:c.493-911C>T , LRG_179t1:c.493-911C>T	NP_922938.1:n.493-911C>T
NM_197948.2:c.492+1023C>T	NP_922939.1:n.492+1023C>T
NM_197949.2:c.354+1023C>T	NP_922940.1:n.354+1023C>T
NM_197950.2:c.256-911C>T	NP_922941.1:n.256-911C>T
NR_125336.1:n.766+813C>T
XM_005253467.3:c.493-911C>T	XP_005253524.1:n.493-911C>T
XM_006719135.2:c.579+813C>T	XP_006719198.1:n.579+813C>T
XR_931351.1:n.159-6807G>A
XR_931352.1:n.159-6807G>A
XM_006719135.3:c.579+813C>T	XP_006719198.1:n.579+813C>T
XM_017019822.1:c.575+817C>T	XP_016875311.1:n.575+817C>T
XM_017019823.1:c.437+817C>T	XP_016875312.1:n.437+817C>T
XM_024449132.1:c.575+817C>T	XP_024304900.1:n.575+817C>T
XM_024449133.1:c.441+813C>T	XP_024304901.1:n.441+813C>T
XR_931351.2:n.160-6807G>A
XR_931352.2:n.160-6807G>A
NM_022570.5:c.355-911C>T	NP_072092.2:n.355-911C>T
NM_197947.3:c.493-911C>T MANE Select	NP_922938.1:n.493-911C>T
NM_197948.3:c.492+1023C>T	NP_922939.1:n.492+1023C>T
NM_197949.3:c.354+1023C>T	NP_922940.1:n.354+1023C>T
NM_197950.3:c.256-911C>T	NP_922941.1:n.256-911C>T
NR_125336.2:n.696+813C>T