Canonical Allele Identifier: CA403124453

Gene: CLEC4M

Linked Data

• COSMIC: COSM6153388 ; COSM6153389 ; COSM6153390
• MyVariant Identifiers: chr19:g.7831630C>A (hg19) ; chr19:g.7766744C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7766744C>A , CM000681.2:g.7766744C>A	GRCh38
NC_000019.9:g.7831630C>A , CM000681.1:g.7831630C>A	GRCh37
NC_000019.8:g.7737630C>A	NCBI36
NG_029190.1:g.8596C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000327325.10:c.873C>A MANE Select	ENSP00000316228.4:p.Asp291Glu
ENST00000359059.10:c.789C>A	ENSP00000351954.6:p.Asp263Glu
ENST00000394122.7:c.789C>A	ENSP00000377680.3:p.Asp263Glu
ENST00000248228.8:c.804C>A	ENSP00000248228.5:p.Asp268Glu
ENST00000327325.9:c.873C>A	ENSP00000316228.4:p.Asp291Glu
ENST00000334806.9:c.720C>A	ENSP00000335228.5:p.Asp240Glu
ENST00000359059.9:c.672C>A	ENSP00000351954.5:p.Asp224Glu
ENST00000394122.6:c.837C>A	ENSP00000377680.2:p.Asp279Glu
ENST00000595496.1:c.465C>A	ENSP00000470132.1:p.Asp155Glu
ENST00000595751.5:c.789C>A	ENSP00000470286.1:p.Asp263Glu
ENST00000596363.5:c.789C>A	ENSP00000471125.1:p.Asp263Glu
ENST00000596707.5:c.672C>A	ENSP00000470137.1:p.Asp224Glu
ENST00000597522.5:c.597C>A	ENSP00000471132.1:p.Asp199Glu
ENST00000598879.5:n.1321C>A
ENST00000599333.1:n.1258C>A
ENST00000601089.1:n.1158C>A
ENST00000602143.1:n.151C>A
NM_001144904.1:c.720C>A	NP_001138376.1:p.Asp240Glu
NM_001144905.1:c.801C>A	NP_001138377.1:p.Asp267Glu
NM_001144906.1:c.465C>A	NP_001138378.1:p.Asp155Glu
NM_001144907.1:c.672C>A	NP_001138379.1:p.Asp224Glu
NM_001144908.1:c.597C>A	NP_001138380.1:p.Asp199Glu
NM_001144909.1:c.735C>A	NP_001138381.1:p.Asp245Glu
NM_001144910.1:c.804C>A	NP_001138382.1:p.Asp268Glu
NM_001144911.1:c.789C>A	NP_001138383.1:p.Asp263Glu
NM_014257.4:c.873C>A	NP_055072.3:p.Asp291Glu
NR_026707.1:n.1439C>A
NR_026708.1:n.1439C>A
NR_026709.1:n.1376C>A
XM_006722611.2:c.870C>A	XP_006722674.1:p.Asp290Glu
XM_006722612.2:c.789C>A	XP_006722675.1:p.Asp263Glu
XM_006722613.2:c.789C>A	XP_006722676.1:p.Asp263Glu
XM_006722614.2:c.705C>A	XP_006722677.1:p.Asp235Glu
XM_006722615.1:c.873C>A	XP_006722678.1:p.Asp291Glu
XR_430125.2:n.991C>A
XR_936147.1:n.991C>A
XM_006722612.3:c.789C>A	XP_006722675.1:p.Asp263Glu
XM_006722613.3:c.789C>A	XP_006722676.1:p.Asp263Glu
XM_006722614.3:c.705C>A	XP_006722677.1:p.Asp235Glu
XM_006722615.2:c.873C>A	XP_006722678.1:p.Asp291Glu
XR_001753583.1:n.1452C>A
XR_001753584.1:n.1158C>A
XR_936147.2:n.991C>A
NM_001144904.2:c.720C>A	NP_001138376.1:p.Asp240Glu
NM_001144905.2:c.801C>A	NP_001138377.1:p.Asp267Glu
NM_001144906.2:c.465C>A	NP_001138378.1:p.Asp155Glu
NM_001144907.2:c.672C>A	NP_001138379.1:p.Asp224Glu
NM_001144908.2:c.597C>A	NP_001138380.1:p.Asp199Glu
NM_001144909.2:c.735C>A	NP_001138381.1:p.Asp245Glu
NM_001144910.2:c.804C>A	NP_001138382.1:p.Asp268Glu
NM_001144911.2:c.789C>A	NP_001138383.1:p.Asp263Glu
NM_014257.5:c.873C>A MANE Select	NP_055072.3:p.Asp291Glu
NR_026707.2:n.1345C>A
NR_026708.2:n.1345C>A
NR_026709.2:n.1282C>A