Canonical Allele Identifier: CA842719455

Gene: CD36

Linked Data

• dbSNP Id: rs1334512
• gnomAD v3: 7-80638588-G-A
• gnomAD v4: 7-80638588-G-A
• MyVariant Identifiers: chr7:g.80267904G>A (hg19) ; chr7:g.80638588G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.80638588G>A , CM000669.2:g.80638588G>A	GRCh38
NC_000007.13:g.80267904G>A , CM000669.1:g.80267904G>A	GRCh37
NC_000007.12:g.80105840G>A	NCBI36
NG_008192.1:g.41401G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000309881.11:c.-183-7500G>A	ENSP00000308165.7:n.-183-7500G>A
ENST00000428497.5:c.-183-7500G>A	ENSP00000409762.1:n.-183-7500G>A
ENST00000433696.6:c.-342G>A	ENSP00000401863.2:n.-342G>A
ENST00000435819.5:c.-183-7500G>A	ENSP00000399421.1:n.-183-7500G>A
ENST00000436384.5:c.-183-7500G>A	ENSP00000398760.1:n.-183-7500G>A
ENST00000438020.5:c.-183-7500G>A	ENSP00000410371.1:n.-183-7500G>A
ENST00000480599.6:n.231-7500G>A
ENST00000526804.5:n.327+1585G>A
ENST00000534394.5:c.-108-17952G>A	ENSP00000431296.1:n.-108-17952G>A
ENST00000538969.5:c.-342G>A	ENSP00000439543.1:n.-342G>A
ENST00000544133.5:c.-342G>A	ENSP00000441956.1:n.-342G>A
NM_000072.3:c.-342G>A	NP_000063.2:n.-342G>A
NM_001001547.2:c.-183-7500G>A	NP_001001547.1:n.-183-7500G>A
NM_001001548.2:c.-342G>A	NP_001001548.1:n.-342G>A
NM_001289911.1:c.-108-17952G>A	NP_001276840.1:n.-108-17952G>A
XM_005250713.1:c.-183-7500G>A	XP_005250770.1:n.-183-7500G>A
XM_005250714.1:c.-183-7500G>A	XP_005250771.1:n.-183-7500G>A
XM_005250715.3:c.-342G>A	XP_005250772.1:n.-342G>A
XM_024447003.1:c.-183-7500G>A	XP_024302771.1:n.-183-7500G>A
NM_001001547.3:c.-183-7500G>A	NP_001001547.1:n.-183-7500G>A
NM_001289911.2:c.-108-17952G>A	NP_001276840.1:n.-108-17952G>A
NM_001371074.1:c.-179-7504G>A	NP_001358003.1:n.-179-7504G>A
NM_001371075.1:c.-183-7500G>A	NP_001358004.1:n.-183-7500G>A
NM_001371077.1:c.-183-7500G>A	NP_001358006.1:n.-183-7500G>A
NM_001371078.1:c.-183-7500G>A	NP_001358007.1:n.-183-7500G>A
NM_001371080.1:c.-184-22475G>A	NP_001358009.1:n.-184-22475G>A
NM_001371081.1:c.-665-7500G>A	NP_001358010.1:n.-665-7500G>A