Canonical Allele Identifier: CA4315463

Gene: CD36

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.80671004C>T , CM000669.2:g.80671004C>T	GRCh38
NC_000007.13:g.80300320C>T , CM000669.1:g.80300320C>T	GRCh37
NC_000007.12:g.80138256C>T	NCBI36
NG_008192.1:g.73817C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001001548.3:c.846C>T MANE Select	NP_001001548.1:p.Asp282=
ENST00000447544.7:c.846C>T MANE Select	ENSP00000415743.2:p.Asp282=
NM_000072.3:c.846C>T	NP_000063.2:p.Asp282=
NM_001001547.2:c.846C>T	NP_001001547.1:p.Asp282=
NM_001001547.3:c.846C>T	NP_001001547.1:p.Asp282=
NM_001001548.2:c.846C>T	NP_001001548.1:p.Asp282=
NM_001127443.1:c.846C>T	NP_001120915.1:p.Asp282=
NM_001127443.2:c.846C>T	NP_001120915.1:p.Asp282=
NM_001127444.1:c.846C>T	NP_001120916.1:p.Asp282=
NM_001127444.2:c.846C>T	NP_001120916.1:p.Asp282=
NM_001289908.1:c.729C>T	NP_001276837.1:p.Asp243=
NM_001289909.1:c.666C>T	NP_001276838.1:p.Asp222=
NM_001289911.1:c.618C>T	NP_001276840.1:p.Asp206=
NM_001289911.2:c.618C>T	NP_001276840.1:p.Asp206=
NM_001371074.1:c.846C>T	NP_001358003.1:p.Asp282=
NM_001371075.1:c.846C>T	NP_001358004.1:p.Asp282=
NM_001371077.1:c.846C>T	NP_001358006.1:p.Asp282=
NM_001371078.1:c.846C>T	NP_001358007.1:p.Asp282=
NM_001371079.1:c.744C>T	NP_001358008.1:p.Asp248=
NM_001371080.1:c.381C>T	NP_001358009.1:p.Asp127=
NM_001371081.1:c.381C>T	NP_001358010.1:p.Asp127=
NR_110501.1:n.998-918C>T
ENST00000309881.11:c.846C>T	ENSP00000308165.7:p.Asp282=
ENST00000394788.7:c.846C>T	ENSP00000378268.3:p.Asp282=
ENST00000419819.2:c.846C>T	ENSP00000392298.2:p.Asp282=
ENST00000432207.5:c.846C>T	ENSP00000411411.1:p.Asp282=
ENST00000433696.6:c.729C>T	ENSP00000401863.2:p.Asp243=
ENST00000435819.5:c.846C>T	ENSP00000399421.1:p.Asp282=
ENST00000447544.6:c.846C>T	ENSP00000415743.2:p.Asp282=
ENST00000464213.1:n.1628C>T
ENST00000534394.5:c.618C>T	ENSP00000431296.1:p.Asp206=
ENST00000538969.5:c.666C>T	ENSP00000439543.1:p.Asp222=
ENST00000544133.5:c.819-918C>T	ENSP00000441956.1:n.819-918C>T
XM_005250713.1:c.846C>T	XP_005250770.1:p.Asp282=
XM_005250714.1:c.846C>T	XP_005250771.1:p.Asp282=
XM_005250715.3:c.846C>T	XP_005250772.1:p.Asp282=
XM_005250715.5:c.846C>T	XP_005250772.1:p.Asp282=
XM_011516707.1:c.846C>T	XP_011515009.1:p.Asp282=
XM_024447002.1:c.846C>T	XP_024302770.1:p.Asp282=
XM_024447003.1:c.846C>T	XP_024302771.1:p.Asp282=