Canonical Allele Identifier: CA3261285854

Gene: CARD11

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.2947705_2947707delinsACC , CM000669.2:g.2947705_2947707delinsACC	GRCh38
NC_000007.13:g.2987339_2987341delinsACC , CM000669.1:g.2987339_2987341delinsACC	GRCh37
NC_000007.12:g.2953865_2953867delinsACC	NCBI36
NG_027759.1:g.101169_101171delinsGGT

Transcript Alleles

HGVS	Amino-acid Change
NM_032415.7:c.88_90delinsGGT MANE Select	NP_115791.3:p.Arg30Gly
ENST00000396946.9:c.88_90delinsGGT MANE Select	ENSP00000380150.4:p.Arg30Gly
NM_001324281.1:c.88_90delinsGGT	NP_001311210.1:p.Arg30Gly
NM_001324281.2:c.88_90delinsGGT	NP_001311210.1:p.Arg30Gly
NM_001324281.3:c.88_90delinsGGT	NP_001311210.1:p.Arg30Gly
NM_032415.5:c.88_90delinsGGT	NP_115791.3:p.Arg30Gly
NM_032415.6:c.88_90delinsGGT	NP_115791.3:p.Arg30Gly
ENST00000356408.3:c.88_90delinsGGT	ENSP00000348779.3:p.Arg30Gly
ENST00000396946.8:c.88_90delinsGGT	ENSP00000380150.4:p.Arg30Gly
ENST00000698637.1:n.414_416delinsGGT
ENST00000698654.1:n.313_315delinsGGT
ENST00000698662.1:n.288_290delinsGGT
XM_011515585.1:c.88_90delinsGGT	XP_011513887.1:p.Arg30Gly
XM_011515586.1:c.88_90delinsGGT	XP_011513888.1:p.Arg30Gly
XM_011515586.2:c.88_90delinsGGT	XP_011513888.1:p.Arg30Gly
XM_011515587.1:c.88_90delinsGGT	XP_011513889.1:p.Arg30Gly
XM_011515587.2:c.88_90delinsGGT	XP_011513889.1:p.Arg30Gly
XR_001744885.1:n.487_489delinsGGT