Canonical Allele Identifier: CA1322088164
Gene: CD28 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203727334A= , CM000664.2:g.203727334A= GRCh38
NC_000002.11:g.204592057A= , CM000664.1:g.204592057A= GRCh37
NC_000002.10:g.204300302A= NCBI36
NG_029618.1:g.25860A=

Transcript Alleles

HGVS Amino-acid change
ENST00000324106.9:c.409+345A= MANE Select ENSP00000324890.7:n.409+345A=
ENST00000324106.8:c.409+345A= ENSP00000324890.7:n.409+345A=
ENST00000374481.7:c.53-2314A= ENSP00000363605.4:n.53-2314A=
ENST00000458610.6:c.451+345A= ENSP00000393648.2:n.451+345A=
NM_001243077.1:c.118+636A= NP_001230006.1:n.118+636A=
NM_001243078.1:c.53-2314A= NP_001230007.1:n.53-2314A=
NM_006139.3:c.409+345A= NP_006130.1:n.409+345A=
XM_006712862.2:c.133+345A= XP_006712925.1:n.133+345A=
XM_011512194.1:c.451+345A= XP_011510496.1:n.451+345A=
XM_011512195.1:c.199+345A= XP_011510497.1:n.199+345A=
XM_011512196.1:c.160+636A= XP_011510498.1:n.160+636A=
XM_011512197.1:c.157+345A= XP_011510499.1:n.157+345A=
XM_011512194.2:c.451+345A= XP_011510496.1:n.451+345A=
XM_011512195.3:c.199+345A= XP_011510497.1:n.199+345A=
XM_011512197.2:c.157+345A= XP_011510499.1:n.157+345A=
NM_006139.4:c.409+345A= MANE Select NP_006130.1:n.409+345A=
NM_001243077.2:c.118+636A= NP_001230006.1:n.118+636A=
NM_001243078.2:c.53-2314A= NP_001230007.1:n.53-2314A=