Canonical Allele Identifier: CA403087669

Gene: CLEC4G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7731709C>T , CM000681.2:g.7731709C>T	GRCh38
NC_000019.9:g.7796595C>T , CM000681.1:g.7796595C>T	GRCh37
NC_000019.8:g.7702595C>T	NCBI36
NG_030321.1:g.5463G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_198492.4:c.118G>A MANE Select	NP_940894.1:p.Val40Ile
ENST00000328853.11:c.118G>A MANE Select	ENSP00000327599.4:p.Val40Ile
NM_001244856.1:c.82G>A	NP_001231785.1:p.Val28Ile
NM_001244856.2:c.82G>A	NP_001231785.1:p.Val28Ile
NM_198492.3:c.118G>A	NP_940894.1:p.Val40Ile
ENST00000328853.10:c.118G>A	ENSP00000327599.4:p.Val40Ile
ENST00000328853.9:c.118G>A	ENSP00000327599.4:p.Val40Ile
ENST00000598081.1:n.180G>A
ENST00000598081.2:n.145G>A
ENST00000599020.1:c.244G>A	ENSP00000472374.1:p.Val82Ile
ENST00000620128.4:c.-231G>A	ENSP00000483109.1:n.-231G>A
ENST00000676543.1:c.443G>A	ENSP00000503143.1:n.443G>A
ENST00000676742.1:c.118G>A	ENSP00000504187.1:p.Val40Ile
ENST00000678003.1:c.849G>A	ENSP00000504497.1:n.849G>A
ENST00000678118.1:c.118G>A	ENSP00000503869.1:p.Val40Ile
ENST00000678780.1:c.2344G>A	ENSP00000503751.1:n.2344G>A
XM_024451485.1:c.118G>A	XP_024307253.1:p.Val40Ile