Canonical Allele Identifier: CA1699802

Gene: CLEC4F

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.70809799C>T , CM000664.2:g.70809799C>T	GRCh38
NC_000002.11:g.71036931C>T , CM000664.1:g.71036931C>T	GRCh37
NC_000002.10:g.70890439C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_173535.3:c.1598G>A MANE Select	NP_775806.2:p.Gly533Asp
ENST00000272367.7:c.1598G>A MANE Select	ENSP00000272367.2:p.Gly533Asp
NM_001258027.1:c.1598G>A	NP_001244956.1:p.Gly533Asp
NM_001258027.2:c.1598G>A	NP_001244956.1:p.Gly533Asp
NM_001321308.1:c.1598G>A	NP_001308237.1:p.Gly533Asp
NM_001321308.2:c.1598G>A	NP_001308237.1:p.Gly533Asp
NM_173535.2:c.1598G>A	NP_775806.2:p.Gly533Asp
ENST00000272367.6:c.1598G>A	ENSP00000272367.2:p.Gly533Asp
ENST00000426626.1:c.1598G>A	ENSP00000390581.1:p.Gly533Asp
XM_005264172.3:c.1598G>A	XP_005264229.1:p.Gly533Asp
XM_011532635.1:c.1928G>A	XP_011530937.1:p.Gly643Asp
XM_011532635.2:c.1928G>A	XP_011530937.1:p.Gly643Asp
XM_011532636.1:c.1928G>A	XP_011530938.1:p.Gly643Asp
XM_011532637.1:c.1928G>A	XP_011530939.1:p.Gly643Asp
XM_011532637.2:c.1928G>A	XP_011530939.1:p.Gly643Asp
XM_011532638.1:c.1928G>A	XP_011530940.1:p.Gly643Asp
XM_011532638.2:c.1928G>A	XP_011530940.1:p.Gly643Asp
XM_011532639.1:c.1928G>A	XP_011530941.1:p.Gly643Asp
XM_011532639.2:c.1928G>A	XP_011530941.1:p.Gly643Asp
XM_011532640.1:c.1928G>A	XP_011530942.1:p.Gly643Asp
XM_011532640.2:c.1928G>A	XP_011530942.1:p.Gly643Asp
XM_011532641.1:c.*33G>A	XP_011530943.1:n.*33G>A
XM_011532641.2:c.*33G>A	XP_011530943.1:n.*33G>A
XM_011532642.1:c.1508G>A	XP_011530944.1:p.Gly503Asp
XM_011532642.2:c.1508G>A	XP_011530944.1:p.Gly503Asp
XM_011532643.1:c.1415G>A	XP_011530945.1:p.Gly472Asp
XM_017003519.1:c.1928G>A	XP_016859008.1:p.Gly643Asp
XR_939671.1:n.2056G>A