Canonical Allele Identifier: CA6443839

Gene: CLEC1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.10098846C>G , CM000674.2:g.10098846C>G	GRCh38
NC_000012.11:g.10251445C>G , CM000674.1:g.10251445C>G	GRCh37
NC_000012.10:g.10142712C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_016511.4:c.77G>C MANE Select	NP_057595.2:p.Gly26Ala
ENST00000315330.8:c.77G>C MANE Select	ENSP00000326407.4:p.Gly26Ala
NM_001297748.1:c.77G>C	NP_001284677.1:p.Gly26Ala
NM_001297748.2:c.77G>C	NP_001284677.1:p.Gly26Ala
NM_001297749.1:c.77G>C	NP_001284678.1:p.Gly26Ala
NM_001297749.2:c.77G>C	NP_001284678.1:p.Gly26Ala
NM_001297750.1:c.-286G>C	NP_001284679.1:n.-286G>C
NM_001297750.2:c.-286G>C	NP_001284679.1:n.-286G>C
NM_001297751.1:c.-230G>C	NP_001284680.1:n.-230G>C
NM_001297751.2:c.-230G>C	NP_001284680.1:n.-230G>C
NM_016511.3:c.77G>C	NP_057595.2:p.Gly26Ala
ENST00000414501.2:c.77G>C	ENSP00000396272.2:p.Gly26Ala
ENST00000420265.2:c.77G>C	ENSP00000417010.2:p.Gly26Ala
ENST00000457018.6:c.77G>C	ENSP00000415048.2:p.Gly26Ala
ENST00000544104.1:c.77G>C	ENSP00000438408.1:p.Gly26Ala
XM_011520687.1:c.77G>C	XP_011518989.1:p.Gly26Ala
XM_011520687.2:c.77G>C	XP_011518989.1:p.Gly26Ala