Canonical Allele Identifier: CA2321083043

Gene: CLEC4M

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7766742G= , CM000681.2:g.7766742G=	GRCh38
NC_000019.9:g.7831628G= , CM000681.1:g.7831628G=	GRCh37
NC_000019.8:g.7737628G=	NCBI36
NG_029190.1:g.8594G=

Transcript Alleles

HGVS	Amino-acid Change
NM_014257.5:c.871G= MANE Select	NP_055072.3:p.Asp291=
ENST00000327325.10:c.871G= MANE Select	ENSP00000316228.4:p.Asp291=
NM_001144904.1:c.718G=	NP_001138376.1:p.Asp240=
NM_001144904.2:c.718G=	NP_001138376.1:p.Asp240=
NM_001144905.1:c.799G=	NP_001138377.1:p.Asp267=
NM_001144905.2:c.799G=	NP_001138377.1:p.Asp267=
NM_001144906.1:c.463G=	NP_001138378.1:p.Asp155=
NM_001144906.2:c.463G=	NP_001138378.1:p.Asp155=
NM_001144907.1:c.670G=	NP_001138379.1:p.Asp224=
NM_001144907.2:c.670G=	NP_001138379.1:p.Asp224=
NM_001144908.1:c.595G=	NP_001138380.1:p.Asp199=
NM_001144908.2:c.595G=	NP_001138380.1:p.Asp199=
NM_001144909.1:c.733G=	NP_001138381.1:p.Asp245=
NM_001144909.2:c.733G=	NP_001138381.1:p.Asp245=
NM_001144910.1:c.802G=	NP_001138382.1:p.Asp268=
NM_001144910.2:c.802G=	NP_001138382.1:p.Asp268=
NM_001144911.1:c.787G=	NP_001138383.1:p.Asp263=
NM_001144911.2:c.787G=	NP_001138383.1:p.Asp263=
NM_014257.4:c.871G=	NP_055072.3:p.Asp291=
NR_026707.1:n.1437G=
NR_026707.2:n.1343G=
NR_026708.1:n.1437G=
NR_026708.2:n.1343G=
NR_026709.1:n.1374G=
NR_026709.2:n.1280G=
ENST00000248228.8:c.802G=	ENSP00000248228.5:p.Asp268=
ENST00000327325.9:c.871G=	ENSP00000316228.4:p.Asp291=
ENST00000334806.9:c.718G=	ENSP00000335228.5:p.Asp240=
ENST00000359059.10:c.787G=	ENSP00000351954.6:p.Asp263=
ENST00000359059.9:c.670G=	ENSP00000351954.5:p.Asp224=
ENST00000394122.6:c.835G=	ENSP00000377680.2:p.Asp279=
ENST00000394122.7:c.787G=	ENSP00000377680.3:p.Asp263=
ENST00000595496.1:c.463G=	ENSP00000470132.1:p.Asp155=
ENST00000595751.5:c.787G=	ENSP00000470286.1:p.Asp263=
ENST00000596363.5:c.787G=	ENSP00000471125.1:p.Asp263=
ENST00000596707.5:c.670G=	ENSP00000470137.1:p.Asp224=
ENST00000597522.5:c.595G=	ENSP00000471132.1:p.Asp199=
ENST00000598879.5:n.1319G=
ENST00000599333.1:n.1256G=
ENST00000601089.1:n.1156G=
ENST00000602143.1:n.149G=
XM_006722611.2:c.868G=	XP_006722674.1:p.Asp290=
XM_006722612.2:c.787G=	XP_006722675.1:p.Asp263=
XM_006722612.3:c.787G=	XP_006722675.1:p.Asp263=
XM_006722613.2:c.787G=	XP_006722676.1:p.Asp263=
XM_006722613.3:c.787G=	XP_006722676.1:p.Asp263=
XM_006722614.2:c.703G=	XP_006722677.1:p.Asp235=
XM_006722614.3:c.703G=	XP_006722677.1:p.Asp235=
XM_006722615.1:c.871G=	XP_006722678.1:p.Asp291=
XM_006722615.2:c.871G=	XP_006722678.1:p.Asp291=
XR_001753583.1:n.1450G=
XR_001753584.1:n.1156G=
XR_430125.2:n.989G=
XR_936147.1:n.989G=
XR_936147.2:n.989G=