Canonical Allele Identifier: CA3261284496

Gene: CARD11

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.2944527_2944528delinsAT , CM000669.2:g.2944527_2944528delinsAT	GRCh38
NC_000007.13:g.2984161_2984162delinsAT , CM000669.1:g.2984161_2984162delinsAT	GRCh37
NC_000007.12:g.2950687_2950688delinsAT	NCBI36
NG_027759.1:g.104348_104349delinsAT

Transcript Alleles

HGVS	Amino-acid Change
NM_032415.7:c.368_369delinsAT MANE Select	NP_115791.3:p.Gly123Asp
ENST00000396946.9:c.368_369delinsAT MANE Select	ENSP00000380150.4:p.Gly123Asp
NM_001324281.1:c.368_369delinsAT	NP_001311210.1:p.Gly123Asp
NM_001324281.2:c.368_369delinsAT	NP_001311210.1:p.Gly123Asp
NM_001324281.3:c.368_369delinsAT	NP_001311210.1:p.Gly123Asp
NM_032415.5:c.368_369delinsAT	NP_115791.3:p.Gly123Asp
NM_032415.6:c.368_369delinsAT	NP_115791.3:p.Gly123Asp
ENST00000396946.8:c.368_369delinsAT	ENSP00000380150.4:p.Gly123Asp
ENST00000698637.1:n.694_695delinsAT
ENST00000698654.1:n.627_628delinsAT
ENST00000698662.1:n.568_569delinsAT
XM_011515585.1:c.368_369delinsAT	XP_011513887.1:p.Gly123Asp
XM_011515586.1:c.368_369delinsAT	XP_011513888.1:p.Gly123Asp
XM_011515586.2:c.368_369delinsAT	XP_011513888.1:p.Gly123Asp
XM_011515587.1:c.368_369delinsAT	XP_011513889.1:p.Gly123Asp
XM_011515587.2:c.368_369delinsAT	XP_011513889.1:p.Gly123Asp
XR_001744885.1:n.767_768delinsAT