Canonical Allele Identifier: CA12542426

Gene: CD36

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.80606698T>G , CM000669.2:g.80606698T>G	GRCh38
NC_000007.13:g.80236014T>G , CM000669.1:g.80236014T>G	GRCh37
NC_000007.12:g.80073950T>G	NCBI36
NG_008192.1:g.9511T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309881.11:c.-184+4319T>G	ENSP00000308165.7:n.-184+4319T>G
ENST00000435819.5:c.-183-39390T>G	ENSP00000399421.1:n.-183-39390T>G
ENST00000480599.6:n.230+4319T>G
ENST00000526804.5:n.155+4319T>G
ENST00000534394.5:c.-109+4319T>G	ENSP00000431296.1:n.-109+4319T>G
NM_001001547.2:c.-184+4319T>G	NP_001001547.1:n.-184+4319T>G
NM_001289911.1:c.-109+4319T>G	NP_001276840.1:n.-109+4319T>G
XM_005250713.1:c.-184+4319T>G	XP_005250770.1:n.-184+4319T>G
XM_024447003.1:c.-184+4319T>G	XP_024302771.1:n.-184+4319T>G
NM_001001547.3:c.-184+4319T>G	NP_001001547.1:n.-184+4319T>G
NM_001289911.2:c.-109+4319T>G	NP_001276840.1:n.-109+4319T>G
NM_001371074.1:c.-180+4319T>G	NP_001358003.1:n.-180+4319T>G
NM_001371075.1:c.-184+4319T>G	NP_001358004.1:n.-184+4319T>G
NM_001371080.1:c.-185+4319T>G	NP_001358009.1:n.-185+4319T>G
NM_001371081.1:c.-666+4319T>G	NP_001358010.1:n.-666+4319T>G