Canonical Allele Identifier: CA161051367

Gene: CD36

Linked Data

• dbSNP Id: rs1056887983
• MyVariant Identifiers: chr7:g.80272545A>G (hg19) ; chr7:g.80643229A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.80643229A>G , CM000669.2:g.80643229A>G	GRCh38
NC_000007.13:g.80272545A>G , CM000669.1:g.80272545A>G	GRCh37
NC_000007.12:g.80110481A>G	NCBI36
NG_008192.1:g.46042A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000447544.7:c.-183-2859A>G MANE Select	ENSP00000415743.2:n.-183-2859A>G
ENST00000309881.11:c.-183-2859A>G	ENSP00000308165.7:n.-183-2859A>G
ENST00000394788.7:c.-183-2859A>G	ENSP00000378268.3:n.-183-2859A>G
ENST00000428497.5:c.-183-2859A>G	ENSP00000409762.1:n.-183-2859A>G
ENST00000433696.6:c.-183-2859A>G	ENSP00000401863.2:n.-183-2859A>G
ENST00000435819.5:c.-183-2859A>G	ENSP00000399421.1:n.-183-2859A>G
ENST00000436384.5:c.-183-2859A>G	ENSP00000398760.1:n.-183-2859A>G
ENST00000438020.5:c.-183-2859A>G	ENSP00000410371.1:n.-183-2859A>G
ENST00000441109.6:n.105-2859A>G
ENST00000447544.6:c.-183-2859A>G	ENSP00000415743.2:n.-183-2859A>G
ENST00000480599.6:n.231-2859A>G
ENST00000482059.6:c.-183-2859A>G	ENSP00000433659.1:n.-183-2859A>G
ENST00000526804.5:n.328-2859A>G
ENST00000534394.5:c.-108-13311A>G	ENSP00000431296.1:n.-108-13311A>G
ENST00000538969.5:c.-183-2859A>G	ENSP00000439543.1:n.-183-2859A>G
ENST00000544133.5:c.-183-2859A>G	ENSP00000441956.1:n.-183-2859A>G
NM_000072.3:c.-183-2859A>G	NP_000063.2:n.-183-2859A>G
NM_001001547.2:c.-183-2859A>G	NP_001001547.1:n.-183-2859A>G
NM_001001548.2:c.-183-2859A>G	NP_001001548.1:n.-183-2859A>G
NM_001289911.1:c.-108-13311A>G	NP_001276840.1:n.-108-13311A>G
XM_005250713.1:c.-183-2859A>G	XP_005250770.1:n.-183-2859A>G
XM_005250714.1:c.-183-2859A>G	XP_005250771.1:n.-183-2859A>G
XM_005250715.3:c.-183-2859A>G	XP_005250772.1:n.-183-2859A>G
XM_005250715.5:c.-183-2859A>G	XP_005250772.1:n.-183-2859A>G
XM_024447002.1:c.-183-2859A>G	XP_024302770.1:n.-183-2859A>G
XM_024447003.1:c.-183-2859A>G	XP_024302771.1:n.-183-2859A>G
NM_001001547.3:c.-183-2859A>G	NP_001001547.1:n.-183-2859A>G
NM_001289911.2:c.-108-13311A>G	NP_001276840.1:n.-108-13311A>G
NM_001371074.1:c.-179-2863A>G	NP_001358003.1:n.-179-2863A>G
NM_001371075.1:c.-183-2859A>G	NP_001358004.1:n.-183-2859A>G
NM_001371077.1:c.-183-2859A>G	NP_001358006.1:n.-183-2859A>G
NM_001371078.1:c.-183-2859A>G	NP_001358007.1:n.-183-2859A>G
NM_001371079.1:c.-183-2859A>G	NP_001358008.1:n.-183-2859A>G
NM_001371080.1:c.-184-17834A>G	NP_001358009.1:n.-184-17834A>G
NM_001371081.1:c.-665-2859A>G	NP_001358010.1:n.-665-2859A>G
NM_001001548.3:c.-183-2859A>G MANE Select	NP_001001548.1:n.-183-2859A>G