Canonical Allele Identifier: CA1720352925
Gene: CD36 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.80657677_80657680delinsAAAG , CM000669.2:g.80657677_80657680delinsAAAG GRCh38
NC_000007.13:g.80286993_80286996delinsAAAG , CM000669.1:g.80286993_80286996delinsAAAG GRCh37
NC_000007.12:g.80124929_80124932delinsAAAG NCBI36
NG_008192.1:g.60490_60493delinsAAAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000447544.7:c.281+977_281+980delinsAAAG MANE Select ENSP00000415743.2:n.281+977_281+980delinsAAAG
ENST00000309881.11:c.281+977_281+980delinsAAAG ENSP00000308165.7:n.281+977_281+980delinsAAAG
ENST00000394788.7:c.281+977_281+980delinsAAAG ENSP00000378268.3:n.281+977_281+980delinsAAAG
ENST00000413265.5:c.281+977_281+980delinsAAAG ENSP00000407690.1:n.281+977_281+980delinsAAAG
ENST00000419819.2:c.281+977_281+980delinsAAAG ENSP00000392298.2:n.281+977_281+980delinsAAAG
ENST00000426978.5:c.281+977_281+980delinsAAAG ENSP00000416388.1:n.281+977_281+980delinsAAAG
ENST00000432207.5:c.281+977_281+980delinsAAAG ENSP00000411411.1:n.281+977_281+980delinsAAAG
ENST00000433696.6:c.281+977_281+980delinsAAAG ENSP00000401863.2:n.281+977_281+980delinsAAAG
ENST00000435819.5:c.281+977_281+980delinsAAAG ENSP00000399421.1:n.281+977_281+980delinsAAAG
ENST00000438020.5:c.281+977_281+980delinsAAAG ENSP00000410371.1:n.281+977_281+980delinsAAAG
ENST00000441034.2:c.241+1017_241+1020delinsAAAG ENSP00000396258.2:n.241+1017_241+1020delinsAAAG
ENST00000447544.6:c.281+977_281+980delinsAAAG ENSP00000415743.2:n.281+977_281+980delinsAAAG
ENST00000534394.5:c.53+977_53+980delinsAAAG ENSP00000431296.1:n.53+977_53+980delinsAAAG
ENST00000538969.5:c.281+977_281+980delinsAAAG ENSP00000439543.1:n.281+977_281+980delinsAAAG
ENST00000544133.5:c.281+977_281+980delinsAAAG ENSP00000441956.1:n.281+977_281+980delinsAAAG
NM_000072.3:c.281+977_281+980delinsAAAG NP_000063.2:n.281+977_281+980delinsAAAG
NM_001001547.2:c.281+977_281+980delinsAAAG NP_001001547.1:n.281+977_281+980delinsAAAG
NM_001001548.2:c.281+977_281+980delinsAAAG NP_001001548.1:n.281+977_281+980delinsAAAG
NM_001127443.1:c.281+977_281+980delinsAAAG NP_001120915.1:n.281+977_281+980delinsAAAG
NM_001127444.1:c.281+977_281+980delinsAAAG NP_001120916.1:n.281+977_281+980delinsAAAG
NM_001289908.1:c.281+977_281+980delinsAAAG NP_001276837.1:n.281+977_281+980delinsAAAG
NM_001289909.1:c.281+977_281+980delinsAAAG NP_001276838.1:n.281+977_281+980delinsAAAG
NM_001289911.1:c.53+977_53+980delinsAAAG NP_001276840.1:n.53+977_53+980delinsAAAG
NR_110501.1:n.460+977_460+980delinsAAAG
XM_005250713.1:c.281+977_281+980delinsAAAG XP_005250770.1:n.281+977_281+980delinsAAAG
XM_005250714.1:c.281+977_281+980delinsAAAG XP_005250771.1:n.281+977_281+980delinsAAAG
XM_005250715.3:c.281+977_281+980delinsAAAG XP_005250772.1:n.281+977_281+980delinsAAAG
XM_011516707.1:c.281+977_281+980delinsAAAG XP_011515009.1:n.281+977_281+980delinsAAAG
XM_005250715.5:c.281+977_281+980delinsAAAG XP_005250772.1:n.281+977_281+980delinsAAAG
XM_024447002.1:c.281+977_281+980delinsAAAG XP_024302770.1:n.281+977_281+980delinsAAAG
XM_024447003.1:c.281+977_281+980delinsAAAG XP_024302771.1:n.281+977_281+980delinsAAAG
NM_001001547.3:c.281+977_281+980delinsAAAG NP_001001547.1:n.281+977_281+980delinsAAAG
NM_001127444.2:c.281+977_281+980delinsAAAG NP_001120916.1:n.281+977_281+980delinsAAAG
NM_001289911.2:c.53+977_53+980delinsAAAG NP_001276840.1:n.53+977_53+980delinsAAAG
NM_001371074.1:c.281+977_281+980delinsAAAG NP_001358003.1:n.281+977_281+980delinsAAAG
NM_001371075.1:c.281+977_281+980delinsAAAG NP_001358004.1:n.281+977_281+980delinsAAAG
NM_001371077.1:c.281+977_281+980delinsAAAG NP_001358006.1:n.281+977_281+980delinsAAAG
NM_001371078.1:c.281+977_281+980delinsAAAG NP_001358007.1:n.281+977_281+980delinsAAAG
NM_001371079.1:c.179+977_179+980delinsAAAG NP_001358008.1:n.179+977_179+980delinsAAAG
NM_001371080.1:c.-184-3386_-184-3383delinsAAAG NP_001358009.1:n.-184-3386_-184-3383delinsAAAG
NM_001371081.1:c.-202+977_-202+980delinsAAAG NP_001358010.1:n.-202+977_-202+980delinsAAAG
NM_001001548.3:c.281+977_281+980delinsAAAG MANE Select NP_001001548.1:n.281+977_281+980delinsAAAG
NM_001127443.2:c.281+977_281+980delinsAAAG NP_001120915.1:n.281+977_281+980delinsAAAG