Canonical Allele Identifier: CA4132035

Gene: CARD11

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.2917286T>C , CM000669.2:g.2917286T>C	GRCh38
NC_000007.13:g.2956920T>C , CM000669.1:g.2956920T>C	GRCh37
NC_000007.12:g.2923446T>C	NCBI36
NG_027759.1:g.131590A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_032415.7:c.2703+4A>G MANE Select	NP_115791.3:n.2703+4A>G
ENST00000396946.9:c.2703+4A>G MANE Select	ENSP00000380150.4:n.2703+4A>G
NM_001324281.1:c.2703+4A>G	NP_001311210.1:n.2703+4A>G
NM_001324281.2:c.2703+4A>G	NP_001311210.1:n.2703+4A>G
NM_001324281.3:c.2703+4A>G	NP_001311210.1:n.2703+4A>G
NM_032415.5:c.2703+4A>G	NP_115791.3:n.2703+4A>G
NM_032415.6:c.2703+4A>G	NP_115791.3:n.2703+4A>G
ENST00000396946.8:c.2703+4A>G	ENSP00000380150.4:n.2703+4A>G
ENST00000698637.1:n.3813+4A>G
ENST00000698652.1:n.1659+4A>G
XM_011515585.1:c.2703+4A>G	XP_011513887.1:n.2703+4A>G
XM_011515586.1:c.2703+4A>G	XP_011513888.1:n.2703+4A>G
XM_011515586.2:c.2703+4A>G	XP_011513888.1:n.2703+4A>G
XM_011515587.1:c.2700+4A>G	XP_011513889.1:n.2700+4A>G
XM_011515587.2:c.2700+4A>G	XP_011513889.1:n.2700+4A>G