Canonical Allele Identifier: CA403123692

Gene: CLEC4M

Linked Data

• MyVariant Identifiers: chr19:g.7831541G>T (hg19) ; chr19:g.7766655G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7766655G>T , CM000681.2:g.7766655G>T	GRCh38
NC_000019.9:g.7831541G>T , CM000681.1:g.7831541G>T	GRCh37
NC_000019.8:g.7737541G>T	NCBI36
NG_029190.1:g.8507G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000327325.10:c.785-1G>T MANE Select	ENSP00000316228.4:n.785-1G>T
ENST00000359059.10:c.701-1G>T	ENSP00000351954.6:n.701-1G>T
ENST00000394122.7:c.701-1G>T	ENSP00000377680.3:n.701-1G>T
ENST00000248228.8:c.716-1G>T	ENSP00000248228.5:n.716-1G>T
ENST00000327325.9:c.785-1G>T	ENSP00000316228.4:n.785-1G>T
ENST00000334806.9:c.632-1G>T	ENSP00000335228.5:n.632-1G>T
ENST00000359059.9:c.584-1G>T	ENSP00000351954.5:n.584-1G>T
ENST00000394122.6:c.749-1G>T	ENSP00000377680.2:n.749-1G>T
ENST00000595496.1:c.377-1G>T	ENSP00000470132.1:n.377-1G>T
ENST00000595751.5:c.701-1G>T	ENSP00000470286.1:n.701-1G>T
ENST00000596363.5:c.701-1G>T	ENSP00000471125.1:n.701-1G>T
ENST00000596707.5:c.584-1G>T	ENSP00000470137.1:n.584-1G>T
ENST00000597522.5:c.509-1G>T	ENSP00000471132.1:n.509-1G>T
ENST00000598879.5:n.1232G>T
ENST00000599333.1:n.1169G>T
ENST00000601089.1:n.1069G>T
ENST00000602143.1:n.62G>T
NM_001144904.1:c.632-1G>T	NP_001138376.1:n.632-1G>T
NM_001144905.1:c.713-1G>T	NP_001138377.1:n.713-1G>T
NM_001144906.1:c.377-1G>T	NP_001138378.1:n.377-1G>T
NM_001144907.1:c.584-1G>T	NP_001138379.1:n.584-1G>T
NM_001144908.1:c.509-1G>T	NP_001138380.1:n.509-1G>T
NM_001144909.1:c.647-1G>T	NP_001138381.1:n.647-1G>T
NM_001144910.1:c.716-1G>T	NP_001138382.1:n.716-1G>T
NM_001144911.1:c.701-1G>T	NP_001138383.1:n.701-1G>T
NM_014257.4:c.785-1G>T	NP_055072.3:n.785-1G>T
NR_026707.1:n.1350G>T
NR_026708.1:n.1350G>T
NR_026709.1:n.1287G>T
XM_006722611.2:c.782-1G>T	XP_006722674.1:n.782-1G>T
XM_006722612.2:c.701-1G>T	XP_006722675.1:n.701-1G>T
XM_006722613.2:c.701-1G>T	XP_006722676.1:n.701-1G>T
XM_006722614.2:c.617-1G>T	XP_006722677.1:n.617-1G>T
XM_006722615.1:c.785-1G>T	XP_006722678.1:n.785-1G>T
XR_430125.2:n.903-1G>T
XR_936147.1:n.903-1G>T
XM_006722612.3:c.701-1G>T	XP_006722675.1:n.701-1G>T
XM_006722613.3:c.701-1G>T	XP_006722676.1:n.701-1G>T
XM_006722614.3:c.617-1G>T	XP_006722677.1:n.617-1G>T
XM_006722615.2:c.785-1G>T	XP_006722678.1:n.785-1G>T
XR_001753583.1:n.1363G>T
XR_001753584.1:n.1069G>T
XR_936147.2:n.903-1G>T
NM_001144904.2:c.632-1G>T	NP_001138376.1:n.632-1G>T
NM_001144905.2:c.713-1G>T	NP_001138377.1:n.713-1G>T
NM_001144906.2:c.377-1G>T	NP_001138378.1:n.377-1G>T
NM_001144907.2:c.584-1G>T	NP_001138379.1:n.584-1G>T
NM_001144908.2:c.509-1G>T	NP_001138380.1:n.509-1G>T
NM_001144909.2:c.647-1G>T	NP_001138381.1:n.647-1G>T
NM_001144910.2:c.716-1G>T	NP_001138382.1:n.716-1G>T
NM_001144911.2:c.701-1G>T	NP_001138383.1:n.701-1G>T
NM_014257.5:c.785-1G>T MANE Select	NP_055072.3:n.785-1G>T
NR_026707.2:n.1256G>T
NR_026708.2:n.1256G>T
NR_026709.2:n.1193G>T