Canonical Allele Identifier: CA2321083048
Gene: CLEC4M HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7766750C= , CM000681.2:g.7766750C= GRCh38
NC_000019.9:g.7831636C= , CM000681.1:g.7831636C= GRCh37
NC_000019.8:g.7737636C= NCBI36
NG_029190.1:g.8602C=

Transcript Alleles

HGVS Amino-acid change
ENST00000327325.10:c.879C= MANE Select ENSP00000316228.4:p.Val293=
ENST00000359059.10:c.795C= ENSP00000351954.6:p.Val265=
ENST00000394122.7:c.795C= ENSP00000377680.3:p.Val265=
ENST00000248228.8:c.810C= ENSP00000248228.5:p.Val270=
ENST00000327325.9:c.879C= ENSP00000316228.4:p.Val293=
ENST00000334806.9:c.726C= ENSP00000335228.5:p.Val242=
ENST00000359059.9:c.678C= ENSP00000351954.5:p.Val226=
ENST00000394122.6:c.843C= ENSP00000377680.2:p.Val281=
ENST00000595496.1:c.471C= ENSP00000470132.1:p.Val157=
ENST00000595751.5:c.795C= ENSP00000470286.1:p.Val265=
ENST00000596363.5:c.795C= ENSP00000471125.1:p.Val265=
ENST00000596707.5:c.678C= ENSP00000470137.1:p.Val226=
ENST00000597522.5:c.603C= ENSP00000471132.1:p.Val201=
ENST00000598879.5:n.1327C=
ENST00000599333.1:n.1264C=
ENST00000601089.1:n.1164C=
ENST00000602143.1:n.157C=
NM_001144904.1:c.726C= NP_001138376.1:p.Val242=
NM_001144905.1:c.807C= NP_001138377.1:p.Val269=
NM_001144906.1:c.471C= NP_001138378.1:p.Val157=
NM_001144907.1:c.678C= NP_001138379.1:p.Val226=
NM_001144908.1:c.603C= NP_001138380.1:p.Val201=
NM_001144909.1:c.741C= NP_001138381.1:p.Val247=
NM_001144910.1:c.810C= NP_001138382.1:p.Val270=
NM_001144911.1:c.795C= NP_001138383.1:p.Val265=
NM_014257.4:c.879C= NP_055072.3:p.Val293=
NR_026707.1:n.1445C=
NR_026708.1:n.1445C=
NR_026709.1:n.1382C=
XM_006722611.2:c.876C= XP_006722674.1:p.Val292=
XM_006722612.2:c.795C= XP_006722675.1:p.Val265=
XM_006722613.2:c.795C= XP_006722676.1:p.Val265=
XM_006722614.2:c.711C= XP_006722677.1:p.Val237=
XM_006722615.1:c.879C= XP_006722678.1:p.Val293=
XR_430125.2:n.997C=
XR_936147.1:n.997C=
XM_006722612.3:c.795C= XP_006722675.1:p.Val265=
XM_006722613.3:c.795C= XP_006722676.1:p.Val265=
XM_006722614.3:c.711C= XP_006722677.1:p.Val237=
XM_006722615.2:c.879C= XP_006722678.1:p.Val293=
XR_001753583.1:n.1458C=
XR_001753584.1:n.1164C=
XR_936147.2:n.997C=
NM_001144904.2:c.726C= NP_001138376.1:p.Val242=
NM_001144905.2:c.807C= NP_001138377.1:p.Val269=
NM_001144906.2:c.471C= NP_001138378.1:p.Val157=
NM_001144907.2:c.678C= NP_001138379.1:p.Val226=
NM_001144908.2:c.603C= NP_001138380.1:p.Val201=
NM_001144909.2:c.741C= NP_001138381.1:p.Val247=
NM_001144910.2:c.810C= NP_001138382.1:p.Val270=
NM_001144911.2:c.795C= NP_001138383.1:p.Val265=
NM_014257.5:c.879C= MANE Select NP_055072.3:p.Val293=
NR_026707.2:n.1351C=
NR_026708.2:n.1351C=
NR_026709.2:n.1288C=