Canonical Allele Identifier: CA2843243745
Gene: CD28 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203707301A>C , CM000664.2:g.203707301A>C GRCh38
NC_000002.11:g.204572024A>C , CM000664.1:g.204572024A>C GRCh37
NC_000002.10:g.204280269A>C NCBI36
NG_029618.1:g.5827A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000324106.9:c.52+553A>C MANE Select ENSP00000324890.7:n.52+553A>C
ENST00000324106.8:c.52+553A>C ENSP00000324890.7:n.52+553A>C
ENST00000374481.7:c.52+553A>C ENSP00000363605.4:n.52+553A>C
ENST00000458610.6:c.94+684A>C ENSP00000393648.2:n.94+684A>C
NM_001243077.1:c.52+553A>C NP_001230006.1:n.52+553A>C
NM_001243078.1:c.52+553A>C NP_001230007.1:n.52+553A>C
NM_006139.3:c.52+553A>C NP_006130.1:n.52+553A>C
XM_006712862.2:c.94+684A>C XP_006712925.1:n.94+684A>C
XM_011512194.1:c.94+684A>C XP_011510496.1:n.94+684A>C
XM_011512195.1:c.94+684A>C XP_011510497.1:n.94+684A>C
XM_011512196.1:c.94+684A>C XP_011510498.1:n.94+684A>C
XM_011512197.1:c.52+553A>C XP_011510499.1:n.52+553A>C
XM_011512194.2:c.94+684A>C XP_011510496.1:n.94+684A>C
XM_011512195.3:c.94+684A>C XP_011510497.1:n.94+684A>C
XM_011512197.2:c.52+553A>C XP_011510499.1:n.52+553A>C
NM_006139.4:c.52+553A>C MANE Select NP_006130.1:n.52+553A>C
NM_001243077.2:c.52+553A>C NP_001230006.1:n.52+553A>C
NM_001243078.2:c.52+553A>C NP_001230007.1:n.52+553A>C