Canonical Allele Identifier: CA1041435558
Gene: CD28 HGNC NCBI

Linked Data

dbSNP Id: rs1693605583

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203721550_203721551del , CM000664.2:g.203721550_203721551del GRCh38
NC_000002.11:g.204586273_204586274del , CM000664.1:g.204586273_204586274del GRCh37
NC_000002.10:g.204294518_204294519del NCBI36
NG_029618.1:g.20076_20077del

Transcript Alleles

HGVS Amino-acid Change
ENST00000324106.9:c.53-5083_53-5082del MANE Select ENSP00000324890.7:n.53-5083_53-5082del
ENST00000324106.8:c.53-5083_53-5082del ENSP00000324890.7:n.53-5083_53-5082del
ENST00000374481.7:c.53-8098_53-8097del ENSP00000363605.4:n.53-8098_53-8097del
ENST00000458610.6:c.95-5083_95-5082del ENSP00000393648.2:n.95-5083_95-5082del
NM_001243077.1:c.53-5083_53-5082del NP_001230006.1:n.53-5083_53-5082del
NM_001243078.1:c.53-8098_53-8097del NP_001230007.1:n.53-8098_53-8097del
NM_006139.3:c.53-5083_53-5082del NP_006130.1:n.53-5083_53-5082del
XM_006712862.2:c.95-5401_95-5400del XP_006712925.1:n.95-5401_95-5400del
XM_011512194.1:c.95-5083_95-5082del XP_011510496.1:n.95-5083_95-5082del
XM_011512195.1:c.95-5083_95-5082del XP_011510497.1:n.95-5083_95-5082del
XM_011512196.1:c.95-5083_95-5082del XP_011510498.1:n.95-5083_95-5082del
XM_011512197.1:c.53-5083_53-5082del XP_011510499.1:n.53-5083_53-5082del
XM_011512194.2:c.95-5083_95-5082del XP_011510496.1:n.95-5083_95-5082del
XM_011512195.3:c.95-5083_95-5082del XP_011510497.1:n.95-5083_95-5082del
XM_011512197.2:c.53-5083_53-5082del XP_011510499.1:n.53-5083_53-5082del
NM_006139.4:c.53-5083_53-5082del MANE Select NP_006130.1:n.53-5083_53-5082del
NM_001243077.2:c.53-5083_53-5082del NP_001230006.1:n.53-5083_53-5082del
NM_001243078.2:c.53-8098_53-8097del NP_001230007.1:n.53-8098_53-8097del