Canonical Allele Identifier: CA1720370787
Gene: CD36 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.80671133T= , CM000669.2:g.80671133T= GRCh38
NC_000007.13:g.80300449T= , CM000669.1:g.80300449T= GRCh37
NC_000007.12:g.80138385T= NCBI36
NG_008192.1:g.73946T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000447544.7:c.975T= MANE Select ENSP00000415743.2:p.Tyr325=
ENST00000309881.11:c.975T= ENSP00000308165.7:p.Tyr325=
ENST00000394788.7:c.975T= ENSP00000378268.3:p.Tyr325=
ENST00000419819.2:c.975T= ENSP00000392298.2:p.Tyr325=
ENST00000432207.5:c.975T= ENSP00000411411.1:p.Tyr325=
ENST00000433696.6:c.858T= ENSP00000401863.2:p.Tyr286=
ENST00000435819.5:c.975T= ENSP00000399421.1:p.Tyr325=
ENST00000447544.6:c.975T= ENSP00000415743.2:p.Tyr325=
ENST00000464213.1:n.1757T=
ENST00000534394.5:c.747T= ENSP00000431296.1:p.Tyr249=
ENST00000538969.5:c.795T= ENSP00000439543.1:p.Tyr265=
ENST00000544133.5:c.819-789T= ENSP00000441956.1:n.819-789T=
NM_000072.3:c.975T= NP_000063.2:p.Tyr325=
NM_001001547.2:c.975T= NP_001001547.1:p.Tyr325=
NM_001001548.2:c.975T= NP_001001548.1:p.Tyr325=
NM_001127443.1:c.975T= NP_001120915.1:p.Tyr325=
NM_001127444.1:c.975T= NP_001120916.1:p.Tyr325=
NM_001289908.1:c.858T= NP_001276837.1:p.Tyr286=
NM_001289909.1:c.795T= NP_001276838.1:p.Tyr265=
NM_001289911.1:c.747T= NP_001276840.1:p.Tyr249=
NR_110501.1:n.998-789T=
XM_005250713.1:c.975T= XP_005250770.1:p.Tyr325=
XM_005250714.1:c.975T= XP_005250771.1:p.Tyr325=
XM_005250715.3:c.975T= XP_005250772.1:p.Tyr325=
XM_011516707.1:c.975T= XP_011515009.1:p.Tyr325=
XM_005250715.5:c.975T= XP_005250772.1:p.Tyr325=
XM_024447002.1:c.975T= XP_024302770.1:p.Tyr325=
XM_024447003.1:c.975T= XP_024302771.1:p.Tyr325=
NM_001001547.3:c.975T= NP_001001547.1:p.Tyr325=
NM_001127444.2:c.975T= NP_001120916.1:p.Tyr325=
NM_001289911.2:c.747T= NP_001276840.1:p.Tyr249=
NM_001371074.1:c.975T= NP_001358003.1:p.Tyr325=
NM_001371075.1:c.975T= NP_001358004.1:p.Tyr325=
NM_001371077.1:c.975T= NP_001358006.1:p.Tyr325=
NM_001371078.1:c.975T= NP_001358007.1:p.Tyr325=
NM_001371079.1:c.873T= NP_001358008.1:p.Tyr291=
NM_001371080.1:c.510T= NP_001358009.1:p.Tyr170=
NM_001371081.1:c.510T= NP_001358010.1:p.Tyr170=
NM_001001548.3:c.975T= MANE Select NP_001001548.1:p.Tyr325=
NM_001127443.2:c.975T= NP_001120915.1:p.Tyr325=