Canonical Allele Identifier: CA1322085571

Gene: CD28

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203721512_203721513delinsTC , CM000664.2:g.203721512_203721513delinsTC	GRCh38
NC_000002.11:g.204586235_204586236delinsTC , CM000664.1:g.204586235_204586236delinsTC	GRCh37
NC_000002.10:g.204294480_204294481delinsTC	NCBI36
NG_029618.1:g.20038_20039delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324106.9:c.53-5121_53-5120delinsTC MANE Select	ENSP00000324890.7:n.53-5121_53-5120delinsTC
ENST00000324106.8:c.53-5121_53-5120delinsTC	ENSP00000324890.7:n.53-5121_53-5120delinsTC
ENST00000374481.7:c.53-8136_53-8135delinsTC	ENSP00000363605.4:n.53-8136_53-8135delinsTC
ENST00000458610.6:c.95-5121_95-5120delinsTC	ENSP00000393648.2:n.95-5121_95-5120delinsTC
NM_001243077.1:c.53-5121_53-5120delinsTC	NP_001230006.1:n.53-5121_53-5120delinsTC
NM_001243078.1:c.53-8136_53-8135delinsTC	NP_001230007.1:n.53-8136_53-8135delinsTC
NM_006139.3:c.53-5121_53-5120delinsTC	NP_006130.1:n.53-5121_53-5120delinsTC
XM_006712862.2:c.95-5439_95-5438delinsTC	XP_006712925.1:n.95-5439_95-5438delinsTC
XM_011512194.1:c.95-5121_95-5120delinsTC	XP_011510496.1:n.95-5121_95-5120delinsTC
XM_011512195.1:c.95-5121_95-5120delinsTC	XP_011510497.1:n.95-5121_95-5120delinsTC
XM_011512196.1:c.95-5121_95-5120delinsTC	XP_011510498.1:n.95-5121_95-5120delinsTC
XM_011512197.1:c.53-5121_53-5120delinsTC	XP_011510499.1:n.53-5121_53-5120delinsTC
XM_011512194.2:c.95-5121_95-5120delinsTC	XP_011510496.1:n.95-5121_95-5120delinsTC
XM_011512195.3:c.95-5121_95-5120delinsTC	XP_011510497.1:n.95-5121_95-5120delinsTC
XM_011512197.2:c.53-5121_53-5120delinsTC	XP_011510499.1:n.53-5121_53-5120delinsTC
NM_006139.4:c.53-5121_53-5120delinsTC MANE Select	NP_006130.1:n.53-5121_53-5120delinsTC
NM_001243077.2:c.53-5121_53-5120delinsTC	NP_001230006.1:n.53-5121_53-5120delinsTC
NM_001243078.2:c.53-8136_53-8135delinsTC	NP_001230007.1:n.53-8136_53-8135delinsTC