Canonical Allele Identifier: CA1720360313

Gene: CD36

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.80629494A= , CM000669.2:g.80629494A=	GRCh38
NC_000007.13:g.80258810A= , CM000669.1:g.80258810A=	GRCh37
NC_000007.12:g.80096746A=	NCBI36
NG_008192.1:g.32307A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309881.11:c.-183-16594A=	ENSP00000308165.7:n.-183-16594A=
ENST00000428497.5:c.-184+3262A=	ENSP00000409762.1:n.-184+3262A=
ENST00000435819.5:c.-183-16594A=	ENSP00000399421.1:n.-183-16594A=
ENST00000436384.5:c.-184+4454A=	ENSP00000398760.1:n.-184+4454A=
ENST00000438020.5:c.-184+5304A=	ENSP00000410371.1:n.-184+5304A=
ENST00000478292.2:n.297-3703A=
ENST00000480599.6:n.231-16594A=
ENST00000526804.5:n.156-7338A=
ENST00000534394.5:c.-108-27046A=	ENSP00000431296.1:n.-108-27046A=
NM_001001547.2:c.-183-16594A=	NP_001001547.1:n.-183-16594A=
NM_001289911.1:c.-108-27046A=	NP_001276840.1:n.-108-27046A=
XM_005250713.1:c.-183-16594A=	XP_005250770.1:n.-183-16594A=
XM_005250714.1:c.-184+5304A=	XP_005250771.1:n.-184+5304A=
XM_024447003.1:c.-183-16594A=	XP_024302771.1:n.-183-16594A=
NM_001001547.3:c.-183-16594A=	NP_001001547.1:n.-183-16594A=
NM_001289911.2:c.-108-27046A=	NP_001276840.1:n.-108-27046A=
NM_001371074.1:c.-179-16598A=	NP_001358003.1:n.-179-16598A=
NM_001371075.1:c.-183-16594A=	NP_001358004.1:n.-183-16594A=
NM_001371077.1:c.-184+5304A=	NP_001358006.1:n.-184+5304A=
NM_001371078.1:c.-184+5304A=	NP_001358007.1:n.-184+5304A=
NM_001371080.1:c.-185+27115A=	NP_001358009.1:n.-185+27115A=
NM_001371081.1:c.-665-16594A=	NP_001358010.1:n.-665-16594A=