Canonical Allele Identifier: CA1322085540

Gene: CD28

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203721433T= , CM000664.2:g.203721433T=	GRCh38
NC_000002.11:g.204586156T= , CM000664.1:g.204586156T=	GRCh37
NC_000002.10:g.204294401T=	NCBI36
NG_029618.1:g.19959T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324106.9:c.53-5200T= MANE Select	ENSP00000324890.7:n.53-5200T=
ENST00000324106.8:c.53-5200T=	ENSP00000324890.7:n.53-5200T=
ENST00000374481.7:c.53-8215T=	ENSP00000363605.4:n.53-8215T=
ENST00000458610.6:c.95-5200T=	ENSP00000393648.2:n.95-5200T=
NM_001243077.1:c.53-5200T=	NP_001230006.1:n.53-5200T=
NM_001243078.1:c.53-8215T=	NP_001230007.1:n.53-8215T=
NM_006139.3:c.53-5200T=	NP_006130.1:n.53-5200T=
XM_006712862.2:c.95-5518T=	XP_006712925.1:n.95-5518T=
XM_011512194.1:c.95-5200T=	XP_011510496.1:n.95-5200T=
XM_011512195.1:c.95-5200T=	XP_011510497.1:n.95-5200T=
XM_011512196.1:c.95-5200T=	XP_011510498.1:n.95-5200T=
XM_011512197.1:c.53-5200T=	XP_011510499.1:n.53-5200T=
XM_011512194.2:c.95-5200T=	XP_011510496.1:n.95-5200T=
XM_011512195.3:c.95-5200T=	XP_011510497.1:n.95-5200T=
XM_011512197.2:c.53-5200T=	XP_011510499.1:n.53-5200T=
NM_006139.4:c.53-5200T= MANE Select	NP_006130.1:n.53-5200T=
NM_001243077.2:c.53-5200T=	NP_001230006.1:n.53-5200T=
NM_001243078.2:c.53-8215T=	NP_001230007.1:n.53-8215T=