Canonical Allele Identifier: CA1322085588
Gene: CD28 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203721543_203721545delinsAAC , CM000664.2:g.203721543_203721545delinsAAC GRCh38
NC_000002.11:g.204586266_204586268delinsAAC , CM000664.1:g.204586266_204586268delinsAAC GRCh37
NC_000002.10:g.204294511_204294513delinsAAC NCBI36
NG_029618.1:g.20069_20071delinsAAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000324106.9:c.53-5090_53-5088delinsAAC MANE Select ENSP00000324890.7:n.53-5090_53-5088delinsAAC
ENST00000324106.8:c.53-5090_53-5088delinsAAC ENSP00000324890.7:n.53-5090_53-5088delinsAAC
ENST00000374481.7:c.53-8105_53-8103delinsAAC ENSP00000363605.4:n.53-8105_53-8103delinsAAC
ENST00000458610.6:c.95-5090_95-5088delinsAAC ENSP00000393648.2:n.95-5090_95-5088delinsAAC
NM_001243077.1:c.53-5090_53-5088delinsAAC NP_001230006.1:n.53-5090_53-5088delinsAAC
NM_001243078.1:c.53-8105_53-8103delinsAAC NP_001230007.1:n.53-8105_53-8103delinsAAC
NM_006139.3:c.53-5090_53-5088delinsAAC NP_006130.1:n.53-5090_53-5088delinsAAC
XM_006712862.2:c.95-5408_95-5406delinsAAC XP_006712925.1:n.95-5408_95-5406delinsAAC
XM_011512194.1:c.95-5090_95-5088delinsAAC XP_011510496.1:n.95-5090_95-5088delinsAAC
XM_011512195.1:c.95-5090_95-5088delinsAAC XP_011510497.1:n.95-5090_95-5088delinsAAC
XM_011512196.1:c.95-5090_95-5088delinsAAC XP_011510498.1:n.95-5090_95-5088delinsAAC
XM_011512197.1:c.53-5090_53-5088delinsAAC XP_011510499.1:n.53-5090_53-5088delinsAAC
XM_011512194.2:c.95-5090_95-5088delinsAAC XP_011510496.1:n.95-5090_95-5088delinsAAC
XM_011512195.3:c.95-5090_95-5088delinsAAC XP_011510497.1:n.95-5090_95-5088delinsAAC
XM_011512197.2:c.53-5090_53-5088delinsAAC XP_011510499.1:n.53-5090_53-5088delinsAAC
NM_006139.4:c.53-5090_53-5088delinsAAC MANE Select NP_006130.1:n.53-5090_53-5088delinsAAC
NM_001243077.2:c.53-5090_53-5088delinsAAC NP_001230006.1:n.53-5090_53-5088delinsAAC
NM_001243078.2:c.53-8105_53-8103delinsAAC NP_001230007.1:n.53-8105_53-8103delinsAAC