Canonical Allele Identifier: CA6443886

Gene: CLEC7A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.10118488A>G , CM000674.2:g.10118488A>G	GRCh38
NC_000012.11:g.10271087A>G , CM000674.1:g.10271087A>G	GRCh37
NC_000012.10:g.10162354A>G	NCBI36
NG_016291.1:g.16782T>C , LRG_179:g.16782T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_197947.3:c.714T>C MANE Select	NP_922938.1:p.Tyr238=
ENST00000304084.13:c.714T>C MANE Select	ENSP00000302569.8:p.Tyr238=
NM_022570.4:c.576T>C	NP_072092.2:p.Tyr192=
NM_022570.5:c.576T>C	NP_072092.2:p.Tyr192=
NM_197947.2:c.714T>C , LRG_179t1:c.714T>C	NP_922938.1:p.Tyr238=
NM_197948.2:c.*25T>C	NP_922939.1:n.*25T>C
NM_197948.3:c.*25T>C	NP_922939.1:n.*25T>C
NM_197949.2:c.*25T>C	NP_922940.1:n.*25T>C
NM_197949.3:c.*25T>C	NP_922940.1:n.*25T>C
NM_197950.2:c.477T>C	NP_922941.1:p.Tyr159=
NM_197950.3:c.477T>C	NP_922941.1:p.Tyr159=
NR_125336.1:n.988T>C
NR_125336.2:n.918T>C
ENST00000298523.9:c.*25T>C	ENSP00000298523.5:n.*25T>C
ENST00000304084.12:c.714T>C	ENSP00000302569.8:p.Tyr238=
ENST00000349926.9:c.325T>C	ENSP00000344723.5:n.325T>C
ENST00000353231.9:c.576T>C	ENSP00000266456.6:p.Tyr192=
ENST00000396484.6:c.477T>C	ENSP00000379743.2:p.Tyr159=
ENST00000465100.5:c.851T>C	ENSP00000436923.1:n.851T>C
ENST00000529761.5:c.714T>C	ENSP00000432876.1:p.Tyr238=
ENST00000533022.5:c.595T>C	ENSP00000431461.1:n.595T>C
ENST00000534609.5:n.2014T>C
XM_005253467.3:c.714T>C	XP_005253524.1:p.Tyr238=
XM_017019822.1:c.678T>C	XP_016875311.1:p.Tyr226=
XM_017019823.1:c.540T>C	XP_016875312.1:p.Tyr180=
XR_931351.1:n.158+2945A>G
XR_931351.2:n.159+2945A>G
XR_931352.1:n.158+2945A>G
XR_931352.2:n.159+2945A>G