Canonical Allele Identifier: CA63683184

Gene: CD28

Linked Data

• dbSNP Id: rs540936067
• gnomAD v2: 2-204585766-AC-A
• gnomAD v3: 2-203721043-AC-A
• gnomAD v4: 2-203721043-AC-A
• MyVariant Identifiers: chr2:g.204585767del (hg19) ; chr2:g.203721044del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203721044del , CM000664.2:g.203721044del	GRCh38
NC_000002.11:g.204585767del , CM000664.1:g.204585767del	GRCh37
NC_000002.10:g.204294012del	NCBI36
NG_029618.1:g.19570del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324106.9:c.53-5589del MANE Select	ENSP00000324890.7:n.53-5589del
ENST00000324106.8:c.53-5589del	ENSP00000324890.7:n.53-5589del
ENST00000374481.7:c.53-8604del	ENSP00000363605.4:n.53-8604del
ENST00000458610.6:c.95-5589del	ENSP00000393648.2:n.95-5589del
NM_001243077.1:c.53-5589del	NP_001230006.1:n.53-5589del
NM_001243078.1:c.53-8604del	NP_001230007.1:n.53-8604del
NM_006139.3:c.53-5589del	NP_006130.1:n.53-5589del
XM_006712862.2:c.95-5907del	XP_006712925.1:n.95-5907del
XM_011512194.1:c.95-5589del	XP_011510496.1:n.95-5589del
XM_011512195.1:c.95-5589del	XP_011510497.1:n.95-5589del
XM_011512196.1:c.95-5589del	XP_011510498.1:n.95-5589del
XM_011512197.1:c.53-5589del	XP_011510499.1:n.53-5589del
XM_011512194.2:c.95-5589del	XP_011510496.1:n.95-5589del
XM_011512195.3:c.95-5589del	XP_011510497.1:n.95-5589del
XM_011512197.2:c.53-5589del	XP_011510499.1:n.53-5589del
NM_006139.4:c.53-5589del MANE Select	NP_006130.1:n.53-5589del
NM_001243077.2:c.53-5589del	NP_001230006.1:n.53-5589del
NM_001243078.2:c.53-8604del	NP_001230007.1:n.53-8604del