Canonical Allele Identifier: CA3261284115

Gene: CARD11

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.2944506_2944508delinsAAT , CM000669.2:g.2944506_2944508delinsAAT	GRCh38
NC_000007.13:g.2984140_2984142delinsAAT , CM000669.1:g.2984140_2984142delinsAAT	GRCh37
NC_000007.12:g.2950666_2950668delinsAAT	NCBI36
NG_027759.1:g.104368_104370delinsATT

Transcript Alleles

HGVS	Amino-acid Change
NM_032415.7:c.388_390delinsATT MANE Select	NP_115791.3:p.Phe130Ile
ENST00000396946.9:c.388_390delinsATT MANE Select	ENSP00000380150.4:p.Phe130Ile
NM_001324281.1:c.388_390delinsATT	NP_001311210.1:p.Phe130Ile
NM_001324281.2:c.388_390delinsATT	NP_001311210.1:p.Phe130Ile
NM_001324281.3:c.388_390delinsATT	NP_001311210.1:p.Phe130Ile
NM_032415.5:c.388_390delinsATT	NP_115791.3:p.Phe130Ile
NM_032415.6:c.388_390delinsATT	NP_115791.3:p.Phe130Ile
ENST00000396946.8:c.388_390delinsATT	ENSP00000380150.4:p.Phe130Ile
ENST00000698637.1:n.714_716delinsATT
ENST00000698654.1:n.647_649delinsATT
ENST00000698662.1:n.588_590delinsATT
XM_011515585.1:c.388_390delinsATT	XP_011513887.1:p.Phe130Ile
XM_011515586.1:c.388_390delinsATT	XP_011513888.1:p.Phe130Ile
XM_011515586.2:c.388_390delinsATT	XP_011513888.1:p.Phe130Ile
XM_011515587.1:c.388_390delinsATT	XP_011513889.1:p.Phe130Ile
XM_011515587.2:c.388_390delinsATT	XP_011513889.1:p.Phe130Ile
XR_001744885.1:n.787_789delinsATT