Canonical Allele Identifier: CA3060588506

Gene: CARD11

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.2947707_2947708delinsAA , CM000669.2:g.2947707_2947708delinsAA	GRCh38
NC_000007.13:g.2987341_2987342delinsAA , CM000669.1:g.2987341_2987342delinsAA	GRCh37
NC_000007.12:g.2953867_2953868delinsAA	NCBI36
NG_027759.1:g.101168_101169delinsTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698637.1:n.413_414delinsTT
ENST00000698654.1:n.312_313delinsTT
ENST00000698662.1:n.287_288delinsTT
ENST00000396946.9:c.87_88delinsTT MANE Select	ENSP00000380150.4:p.Arg30Trp
ENST00000356408.3:c.87_88delinsTT	ENSP00000348779.3:p.Arg30Trp
ENST00000396946.8:c.87_88delinsTT	ENSP00000380150.4:p.Arg30Trp
NM_032415.5:c.87_88delinsTT	NP_115791.3:p.Arg30Trp
XM_011515585.1:c.87_88delinsTT	XP_011513887.1:p.Arg30Trp
XM_011515586.1:c.87_88delinsTT	XP_011513888.1:p.Arg30Trp
XM_011515587.1:c.87_88delinsTT	XP_011513889.1:p.Arg30Trp
NM_001324281.1:c.87_88delinsTT	NP_001311210.1:p.Arg30Trp
XM_011515586.2:c.87_88delinsTT	XP_011513888.1:p.Arg30Trp
XM_011515587.2:c.87_88delinsTT	XP_011513889.1:p.Arg30Trp
XR_001744885.1:n.486_487delinsTT
NM_001324281.2:c.87_88delinsTT	NP_001311210.1:p.Arg30Trp
NM_032415.6:c.87_88delinsTT	NP_115791.3:p.Arg30Trp
NM_001324281.3:c.87_88delinsTT	NP_001311210.1:p.Arg30Trp
NM_032415.7:c.87_88delinsTT MANE Select	NP_115791.3:p.Arg30Trp