Canonical Allele Identifier: CA3261284488

Gene: CARD11

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.2944527_2944529delinsACT , CM000669.2:g.2944527_2944529delinsACT	GRCh38
NC_000007.13:g.2984161_2984163delinsACT , CM000669.1:g.2984161_2984163delinsACT	GRCh37
NC_000007.12:g.2950687_2950689delinsACT	NCBI36
NG_027759.1:g.104347_104349delinsAGT

Transcript Alleles

HGVS	Amino-acid Change
NM_032415.7:c.367_369delinsAGT MANE Select	NP_115791.3:p.Gly123Ser
ENST00000396946.9:c.367_369delinsAGT MANE Select	ENSP00000380150.4:p.Gly123Ser
NM_001324281.1:c.367_369delinsAGT	NP_001311210.1:p.Gly123Ser
NM_001324281.2:c.367_369delinsAGT	NP_001311210.1:p.Gly123Ser
NM_001324281.3:c.367_369delinsAGT	NP_001311210.1:p.Gly123Ser
NM_032415.5:c.367_369delinsAGT	NP_115791.3:p.Gly123Ser
NM_032415.6:c.367_369delinsAGT	NP_115791.3:p.Gly123Ser
ENST00000396946.8:c.367_369delinsAGT	ENSP00000380150.4:p.Gly123Ser
ENST00000698637.1:n.693_695delinsAGT
ENST00000698654.1:n.626_628delinsAGT
ENST00000698662.1:n.567_569delinsAGT
XM_011515585.1:c.367_369delinsAGT	XP_011513887.1:p.Gly123Ser
XM_011515586.1:c.367_369delinsAGT	XP_011513888.1:p.Gly123Ser
XM_011515586.2:c.367_369delinsAGT	XP_011513888.1:p.Gly123Ser
XM_011515587.1:c.367_369delinsAGT	XP_011513889.1:p.Gly123Ser
XM_011515587.2:c.367_369delinsAGT	XP_011513889.1:p.Gly123Ser
XR_001744885.1:n.766_768delinsAGT