Canonical Allele Identifier: CA1322077277

Gene: CD28

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203707364C= , CM000664.2:g.203707364C=	GRCh38
NC_000002.11:g.204572087C= , CM000664.1:g.204572087C=	GRCh37
NC_000002.10:g.204280332C=	NCBI36
NG_029618.1:g.5890C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000324106.9:c.52+616C= MANE Select	ENSP00000324890.7:n.52+616C=
ENST00000324106.8:c.52+616C=	ENSP00000324890.7:n.52+616C=
ENST00000374481.7:c.52+616C=	ENSP00000363605.4:n.52+616C=
ENST00000458610.6:c.94+747C=	ENSP00000393648.2:n.94+747C=
NM_001243077.1:c.52+616C=	NP_001230006.1:n.52+616C=
NM_001243078.1:c.52+616C=	NP_001230007.1:n.52+616C=
NM_006139.3:c.52+616C=	NP_006130.1:n.52+616C=
XM_006712862.2:c.94+747C=	XP_006712925.1:n.94+747C=
XM_011512194.1:c.94+747C=	XP_011510496.1:n.94+747C=
XM_011512195.1:c.94+747C=	XP_011510497.1:n.94+747C=
XM_011512196.1:c.94+747C=	XP_011510498.1:n.94+747C=
XM_011512197.1:c.52+616C=	XP_011510499.1:n.52+616C=
XM_011512194.2:c.94+747C=	XP_011510496.1:n.94+747C=
XM_011512195.3:c.94+747C=	XP_011510497.1:n.94+747C=
XM_011512197.2:c.52+616C=	XP_011510499.1:n.52+616C=
NM_006139.4:c.52+616C= MANE Select	NP_006130.1:n.52+616C=
NM_001243077.2:c.52+616C=	NP_001230006.1:n.52+616C=
NM_001243078.2:c.52+616C=	NP_001230007.1:n.52+616C=