Canonical Allele Identifier: CA4315245

Gene: CD36

Linked Data

• ClinVar Variation Id: 910699
• ClinVar RCV Id: RCV001162669
• dbSNP Id: rs141680676
• ExAC: 7:80292467 A / T
• gnomAD v2: 7-80292467-A-T
• gnomAD v3: 7-80663151-A-T
• gnomAD v4: 7-80663151-A-T
• MyVariant Identifiers: chr7:g.80292467A>T (hg19) ; chr7:g.80663151A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.80663151A>T , CM000669.2:g.80663151A>T	GRCh38
NC_000007.13:g.80292467A>T , CM000669.1:g.80292467A>T	GRCh37
NC_000007.12:g.80130403A>T	NCBI36
NG_008192.1:g.65964A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000447544.7:c.591A>T MANE Select	ENSP00000415743.2:p.Thr197=
ENST00000309881.11:c.591A>T	ENSP00000308165.7:p.Thr197=
ENST00000394788.7:c.591A>T	ENSP00000378268.3:p.Thr197=
ENST00000413265.5:c.591A>T	ENSP00000407690.1:p.Thr197=
ENST00000419819.2:c.591A>T	ENSP00000392298.2:p.Thr197=
ENST00000432207.5:c.591A>T	ENSP00000411411.1:p.Thr197=
ENST00000433696.6:c.591A>T	ENSP00000401863.2:p.Thr197=
ENST00000435819.5:c.591A>T	ENSP00000399421.1:p.Thr197=
ENST00000441034.2:c.*103A>T	ENSP00000396258.2:n.*103A>T
ENST00000447544.6:c.591A>T	ENSP00000415743.2:p.Thr197=
ENST00000534394.5:c.363A>T	ENSP00000431296.1:p.Thr121=
ENST00000538969.5:c.430-1255A>T	ENSP00000439543.1:n.430-1255A>T
ENST00000544133.5:c.591A>T	ENSP00000441956.1:p.Thr197=
NM_000072.3:c.591A>T	NP_000063.2:p.Thr197=
NM_001001547.2:c.591A>T	NP_001001547.1:p.Thr197=
NM_001001548.2:c.591A>T	NP_001001548.1:p.Thr197=
NM_001127443.1:c.591A>T	NP_001120915.1:p.Thr197=
NM_001127444.1:c.591A>T	NP_001120916.1:p.Thr197=
NM_001289908.1:c.591A>T	NP_001276837.1:p.Thr197=
NM_001289909.1:c.430-1255A>T	NP_001276838.1:n.430-1255A>T
NM_001289911.1:c.363A>T	NP_001276840.1:p.Thr121=
NR_110501.1:n.770A>T
XM_005250713.1:c.591A>T	XP_005250770.1:p.Thr197=
XM_005250714.1:c.591A>T	XP_005250771.1:p.Thr197=
XM_005250715.3:c.591A>T	XP_005250772.1:p.Thr197=
XM_011516707.1:c.591A>T	XP_011515009.1:p.Thr197=
XM_005250715.5:c.591A>T	XP_005250772.1:p.Thr197=
XM_024447002.1:c.591A>T	XP_024302770.1:p.Thr197=
XM_024447003.1:c.591A>T	XP_024302771.1:p.Thr197=
NM_001001547.3:c.591A>T	NP_001001547.1:p.Thr197=
NM_001127444.2:c.591A>T	NP_001120916.1:p.Thr197=
NM_001289911.2:c.363A>T	NP_001276840.1:p.Thr121=
NM_001371074.1:c.591A>T	NP_001358003.1:p.Thr197=
NM_001371075.1:c.591A>T	NP_001358004.1:p.Thr197=
NM_001371077.1:c.591A>T	NP_001358006.1:p.Thr197=
NM_001371078.1:c.591A>T	NP_001358007.1:p.Thr197=
NM_001371079.1:c.489A>T	NP_001358008.1:p.Thr163=
NM_001371080.1:c.126A>T	NP_001358009.1:p.Thr42=
NM_001371081.1:c.126A>T	NP_001358010.1:p.Thr42=
NM_001001548.3:c.591A>T MANE Select	NP_001001548.1:p.Thr197=
NM_001127443.2:c.591A>T	NP_001120915.1:p.Thr197=