Canonical Allele Identifier: CA161064490

Gene: CD36

Linked Data

• dbSNP Id: rs989710862
• gnomAD v3: 7-80657649-ACT-A
• gnomAD v4: 7-80657649-ACT-A
• MyVariant Identifiers: chr7:g.80286966_80286967del (hg19) ; chr7:g.80657650_80657651del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.80657652_80657653del , CM000669.2:g.80657652_80657653del	GRCh38
NC_000007.13:g.80286968_80286969del , CM000669.1:g.80286968_80286969del	GRCh37
NC_000007.12:g.80124904_80124905del	NCBI36
NG_008192.1:g.60465_60466del

Transcript Alleles

HGVS	Amino-acid change
ENST00000447544.7:c.281+952_281+953del MANE Select	ENSP00000415743.2:n.281+952_281+953del
ENST00000309881.11:c.281+952_281+953del	ENSP00000308165.7:n.281+952_281+953del
ENST00000394788.7:c.281+952_281+953del	ENSP00000378268.3:n.281+952_281+953del
ENST00000413265.5:c.281+952_281+953del	ENSP00000407690.1:n.281+952_281+953del
ENST00000419819.2:c.281+952_281+953del	ENSP00000392298.2:n.281+952_281+953del
ENST00000426978.5:c.281+952_281+953del	ENSP00000416388.1:n.281+952_281+953del
ENST00000432207.5:c.281+952_281+953del	ENSP00000411411.1:n.281+952_281+953del
ENST00000433696.6:c.281+952_281+953del	ENSP00000401863.2:n.281+952_281+953del
ENST00000435819.5:c.281+952_281+953del	ENSP00000399421.1:n.281+952_281+953del
ENST00000438020.5:c.281+952_281+953del	ENSP00000410371.1:n.281+952_281+953del
ENST00000441034.2:c.241+992_241+993del	ENSP00000396258.2:n.241+992_241+993del
ENST00000447544.6:c.281+952_281+953del	ENSP00000415743.2:n.281+952_281+953del
ENST00000534394.5:c.53+952_53+953del	ENSP00000431296.1:n.53+952_53+953del
ENST00000538969.5:c.281+952_281+953del	ENSP00000439543.1:n.281+952_281+953del
ENST00000544133.5:c.281+952_281+953del	ENSP00000441956.1:n.281+952_281+953del
NM_000072.3:c.281+952_281+953del	NP_000063.2:n.281+952_281+953del
NM_001001547.2:c.281+952_281+953del	NP_001001547.1:n.281+952_281+953del
NM_001001548.2:c.281+952_281+953del	NP_001001548.1:n.281+952_281+953del
NM_001127443.1:c.281+952_281+953del	NP_001120915.1:n.281+952_281+953del
NM_001127444.1:c.281+952_281+953del	NP_001120916.1:n.281+952_281+953del
NM_001289908.1:c.281+952_281+953del	NP_001276837.1:n.281+952_281+953del
NM_001289909.1:c.281+952_281+953del	NP_001276838.1:n.281+952_281+953del
NM_001289911.1:c.53+952_53+953del	NP_001276840.1:n.53+952_53+953del
NR_110501.1:n.460+952_460+953del
XM_005250713.1:c.281+952_281+953del	XP_005250770.1:n.281+952_281+953del
XM_005250714.1:c.281+952_281+953del	XP_005250771.1:n.281+952_281+953del
XM_005250715.3:c.281+952_281+953del	XP_005250772.1:n.281+952_281+953del
XM_011516707.1:c.281+952_281+953del	XP_011515009.1:n.281+952_281+953del
XM_005250715.5:c.281+952_281+953del	XP_005250772.1:n.281+952_281+953del
XM_024447002.1:c.281+952_281+953del	XP_024302770.1:n.281+952_281+953del
XM_024447003.1:c.281+952_281+953del	XP_024302771.1:n.281+952_281+953del
NM_001001547.3:c.281+952_281+953del	NP_001001547.1:n.281+952_281+953del
NM_001127444.2:c.281+952_281+953del	NP_001120916.1:n.281+952_281+953del
NM_001289911.2:c.53+952_53+953del	NP_001276840.1:n.53+952_53+953del
NM_001371074.1:c.281+952_281+953del	NP_001358003.1:n.281+952_281+953del
NM_001371075.1:c.281+952_281+953del	NP_001358004.1:n.281+952_281+953del
NM_001371077.1:c.281+952_281+953del	NP_001358006.1:n.281+952_281+953del
NM_001371078.1:c.281+952_281+953del	NP_001358007.1:n.281+952_281+953del
NM_001371079.1:c.179+952_179+953del	NP_001358008.1:n.179+952_179+953del
NM_001371080.1:c.-184-3411_-184-3410del	NP_001358009.1:n.-184-3411_-184-3410del
NM_001371081.1:c.-202+952_-202+953del	NP_001358010.1:n.-202+952_-202+953del
NM_001001548.3:c.281+952_281+953del MANE Select	NP_001001548.1:n.281+952_281+953del
NM_001127443.2:c.281+952_281+953del	NP_001120915.1:n.281+952_281+953del