Canonical Allele Identifier: CA366647331

Gene: CARD11

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.2944538C>T , CM000669.2:g.2944538C>T	GRCh38
NC_000007.13:g.2984172C>T , CM000669.1:g.2984172C>T	GRCh37
NC_000007.12:g.2950698C>T	NCBI36
NG_027759.1:g.104338G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_032415.7:c.359-1G>A MANE Select	NP_115791.3:n.359-1G>A
ENST00000396946.9:c.359-1G>A MANE Select	ENSP00000380150.4:n.359-1G>A
NM_001324281.1:c.359-1G>A	NP_001311210.1:n.359-1G>A
NM_001324281.2:c.359-1G>A	NP_001311210.1:n.359-1G>A
NM_001324281.3:c.359-1G>A	NP_001311210.1:n.359-1G>A
NM_032415.5:c.359-1G>A	NP_115791.3:n.359-1G>A
NM_032415.6:c.359-1G>A	NP_115791.3:n.359-1G>A
ENST00000396946.8:c.359-1G>A	ENSP00000380150.4:n.359-1G>A
ENST00000698637.1:n.685-1G>A
ENST00000698654.1:n.617G>A
ENST00000698662.1:n.559-1G>A
XM_011515585.1:c.359-1G>A	XP_011513887.1:n.359-1G>A
XM_011515586.1:c.359-1G>A	XP_011513888.1:n.359-1G>A
XM_011515586.2:c.359-1G>A	XP_011513888.1:n.359-1G>A
XM_011515587.1:c.359-1G>A	XP_011513889.1:n.359-1G>A
XM_011515587.2:c.359-1G>A	XP_011513889.1:n.359-1G>A
XR_001744885.1:n.758-1G>A