Canonical Allele Identifier: CA505232308

Gene: CLEC4M

Linked Data

• gnomAD v4: 19-7766657-A-G
• MyVariant Identifiers: chr19:g.7831543A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7766657A>G , CM000681.2:g.7766657A>G	GRCh38
NC_000019.9:g.7831543A>G , CM000681.1:g.7831543A>G	GRCh37
NC_000019.8:g.7737543A>G	NCBI36
NG_029190.1:g.8509A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000327325.10:c.786A>G MANE Select	ENSP00000316228.4:p.Glu262=
ENST00000359059.10:c.702A>G	ENSP00000351954.6:p.Glu234=
ENST00000394122.7:c.702A>G	ENSP00000377680.3:p.Glu234=
ENST00000248228.8:c.717A>G	ENSP00000248228.5:p.Glu239=
ENST00000327325.9:c.786A>G	ENSP00000316228.4:p.Glu262=
ENST00000334806.9:c.633A>G	ENSP00000335228.5:p.Glu211=
ENST00000359059.9:c.585A>G	ENSP00000351954.5:p.Glu195=
ENST00000394122.6:c.750A>G	ENSP00000377680.2:p.Glu250=
ENST00000595496.1:c.378A>G	ENSP00000470132.1:p.Glu126=
ENST00000595751.5:c.702A>G	ENSP00000470286.1:p.Glu234=
ENST00000596363.5:c.702A>G	ENSP00000471125.1:p.Glu234=
ENST00000596707.5:c.585A>G	ENSP00000470137.1:p.Glu195=
ENST00000597522.5:c.510A>G	ENSP00000471132.1:p.Glu170=
ENST00000598879.5:n.1234A>G
ENST00000599333.1:n.1171A>G
ENST00000601089.1:n.1071A>G
ENST00000602143.1:n.64A>G
NM_001144904.1:c.633A>G	NP_001138376.1:p.Glu211=
NM_001144905.1:c.714A>G	NP_001138377.1:p.Glu238=
NM_001144906.1:c.378A>G	NP_001138378.1:p.Glu126=
NM_001144907.1:c.585A>G	NP_001138379.1:p.Glu195=
NM_001144908.1:c.510A>G	NP_001138380.1:p.Glu170=
NM_001144909.1:c.648A>G	NP_001138381.1:p.Glu216=
NM_001144910.1:c.717A>G	NP_001138382.1:p.Glu239=
NM_001144911.1:c.702A>G	NP_001138383.1:p.Glu234=
NM_014257.4:c.786A>G	NP_055072.3:p.Glu262=
NR_026707.1:n.1352A>G
NR_026708.1:n.1352A>G
NR_026709.1:n.1289A>G
XM_006722611.2:c.783A>G	XP_006722674.1:p.Glu261=
XM_006722612.2:c.702A>G	XP_006722675.1:p.Glu234=
XM_006722613.2:c.702A>G	XP_006722676.1:p.Glu234=
XM_006722614.2:c.618A>G	XP_006722677.1:p.Glu206=
XM_006722615.1:c.786A>G	XP_006722678.1:p.Glu262=
XR_430125.2:n.904A>G
XR_936147.1:n.904A>G
XM_006722612.3:c.702A>G	XP_006722675.1:p.Glu234=
XM_006722613.3:c.702A>G	XP_006722676.1:p.Glu234=
XM_006722614.3:c.618A>G	XP_006722677.1:p.Glu206=
XM_006722615.2:c.786A>G	XP_006722678.1:p.Glu262=
XR_001753583.1:n.1365A>G
XR_001753584.1:n.1071A>G
XR_936147.2:n.904A>G
NM_001144904.2:c.633A>G	NP_001138376.1:p.Glu211=
NM_001144905.2:c.714A>G	NP_001138377.1:p.Glu238=
NM_001144906.2:c.378A>G	NP_001138378.1:p.Glu126=
NM_001144907.2:c.585A>G	NP_001138379.1:p.Glu195=
NM_001144908.2:c.510A>G	NP_001138380.1:p.Glu170=
NM_001144909.2:c.648A>G	NP_001138381.1:p.Glu216=
NM_001144910.2:c.717A>G	NP_001138382.1:p.Glu239=
NM_001144911.2:c.702A>G	NP_001138383.1:p.Glu234=
NM_014257.5:c.786A>G MANE Select	NP_055072.3:p.Glu262=
NR_026707.2:n.1258A>G
NR_026708.2:n.1258A>G
NR_026709.2:n.1195A>G