Canonical Allele Identifier: CA366647339

Gene: CARD11 CARD11-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.2945818C>T , CM000669.2:g.2945818C>T	GRCh38
NC_000007.13:g.2985452C>T , CM000669.1:g.2985452C>T	GRCh37
NC_000007.12:g.2951978C>T	NCBI36
NG_027759.1:g.103058G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_032415.7:c.358+1G>A (CARD11) MANE Select	NP_115791.3:n.358+1G>A
ENST00000396946.9:c.358+1G>A (CARD11) MANE Select	ENSP00000380150.4:n.358+1G>A
NM_001324281.1:c.358+1G>A (CARD11)	NP_001311210.1:n.358+1G>A
NM_001324281.2:c.358+1G>A (CARD11)	NP_001311210.1:n.358+1G>A
NM_001324281.3:c.358+1G>A (CARD11)	NP_001311210.1:n.358+1G>A
NM_032415.5:c.358+1G>A (CARD11)	NP_115791.3:n.358+1G>A
NM_032415.6:c.358+1G>A (CARD11)	NP_115791.3:n.358+1G>A
ENST00000396946.8:c.358+1G>A (CARD11)	ENSP00000380150.4:n.358+1G>A
ENST00000698637.1:n.684+1G>A (CARD11)
ENST00000698654.1:n.583+1G>A (CARD11)
ENST00000698662.1:n.558+1G>A (CARD11)
XM_011515585.1:c.358+1G>A (CARD11)	XP_011513887.1:n.358+1G>A
XM_011515586.1:c.358+1G>A (CARD11)	XP_011513888.1:n.358+1G>A
XM_011515586.2:c.358+1G>A (CARD11)	XP_011513888.1:n.358+1G>A
XM_011515587.1:c.358+1G>A (CARD11)	XP_011513889.1:n.358+1G>A
XM_011515587.2:c.358+1G>A (CARD11)	XP_011513889.1:n.358+1G>A
XR_001744885.1:n.757+1G>A (CARD11)
XR_926993.1:n.57-779C>T (CARD11-AS1)