Canonical Allele Identifier: CA2321083006
Gene: CLEC4M HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7766658C= , CM000681.2:g.7766658C= GRCh38
NC_000019.9:g.7831544C= , CM000681.1:g.7831544C= GRCh37
NC_000019.8:g.7737544C= NCBI36
NG_029190.1:g.8510C=

Transcript Alleles

HGVS Amino-acid change
ENST00000327325.10:c.787C= MANE Select ENSP00000316228.4:p.Arg263=
ENST00000359059.10:c.703C= ENSP00000351954.6:p.Arg235=
ENST00000394122.7:c.703C= ENSP00000377680.3:p.Arg235=
ENST00000248228.8:c.718C= ENSP00000248228.5:p.Arg240=
ENST00000327325.9:c.787C= ENSP00000316228.4:p.Arg263=
ENST00000334806.9:c.634C= ENSP00000335228.5:p.Arg212=
ENST00000359059.9:c.586C= ENSP00000351954.5:p.Arg196=
ENST00000394122.6:c.751C= ENSP00000377680.2:p.Arg251=
ENST00000595496.1:c.379C= ENSP00000470132.1:p.Arg127=
ENST00000595751.5:c.703C= ENSP00000470286.1:p.Arg235=
ENST00000596363.5:c.703C= ENSP00000471125.1:p.Arg235=
ENST00000596707.5:c.586C= ENSP00000470137.1:p.Arg196=
ENST00000597522.5:c.511C= ENSP00000471132.1:p.Arg171=
ENST00000598879.5:n.1235C=
ENST00000599333.1:n.1172C=
ENST00000601089.1:n.1072C=
ENST00000602143.1:n.65C=
NM_001144904.1:c.634C= NP_001138376.1:p.Arg212=
NM_001144905.1:c.715C= NP_001138377.1:p.Arg239=
NM_001144906.1:c.379C= NP_001138378.1:p.Arg127=
NM_001144907.1:c.586C= NP_001138379.1:p.Arg196=
NM_001144908.1:c.511C= NP_001138380.1:p.Arg171=
NM_001144909.1:c.649C= NP_001138381.1:p.Arg217=
NM_001144910.1:c.718C= NP_001138382.1:p.Arg240=
NM_001144911.1:c.703C= NP_001138383.1:p.Arg235=
NM_014257.4:c.787C= NP_055072.3:p.Arg263=
NR_026707.1:n.1353C=
NR_026708.1:n.1353C=
NR_026709.1:n.1290C=
XM_006722611.2:c.784C= XP_006722674.1:p.Arg262=
XM_006722612.2:c.703C= XP_006722675.1:p.Arg235=
XM_006722613.2:c.703C= XP_006722676.1:p.Arg235=
XM_006722614.2:c.619C= XP_006722677.1:p.Arg207=
XM_006722615.1:c.787C= XP_006722678.1:p.Arg263=
XR_430125.2:n.905C=
XR_936147.1:n.905C=
XM_006722612.3:c.703C= XP_006722675.1:p.Arg235=
XM_006722613.3:c.703C= XP_006722676.1:p.Arg235=
XM_006722614.3:c.619C= XP_006722677.1:p.Arg207=
XM_006722615.2:c.787C= XP_006722678.1:p.Arg263=
XR_001753583.1:n.1366C=
XR_001753584.1:n.1072C=
XR_936147.2:n.905C=
NM_001144904.2:c.634C= NP_001138376.1:p.Arg212=
NM_001144905.2:c.715C= NP_001138377.1:p.Arg239=
NM_001144906.2:c.379C= NP_001138378.1:p.Arg127=
NM_001144907.2:c.586C= NP_001138379.1:p.Arg196=
NM_001144908.2:c.511C= NP_001138380.1:p.Arg171=
NM_001144909.2:c.649C= NP_001138381.1:p.Arg217=
NM_001144910.2:c.718C= NP_001138382.1:p.Arg240=
NM_001144911.2:c.703C= NP_001138383.1:p.Arg235=
NM_014257.5:c.787C= MANE Select NP_055072.3:p.Arg263=
NR_026707.2:n.1259C=
NR_026708.2:n.1259C=
NR_026709.2:n.1196C=