Canonical Allele Identifier: CA572195325

Gene: CARD11

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.2937897G>C , CM000669.2:g.2937897G>C	GRCh38
NC_000007.13:g.2977531G>C , CM000669.1:g.2977531G>C	GRCh37
NC_000007.12:g.2944057G>C	NCBI36
NG_027759.1:g.110979C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_032415.7:c.1143+10C>G MANE Select	NP_115791.3:n.1143+10C>G
ENST00000396946.9:c.1143+10C>G MANE Select	ENSP00000380150.4:n.1143+10C>G
NM_001324281.1:c.1143+10C>G	NP_001311210.1:n.1143+10C>G
NM_001324281.2:c.1143+10C>G	NP_001311210.1:n.1143+10C>G
NM_001324281.3:c.1143+10C>G	NP_001311210.1:n.1143+10C>G
NM_032415.5:c.1143+10C>G	NP_115791.3:n.1143+10C>G
NM_032415.6:c.1143+10C>G	NP_115791.3:n.1143+10C>G
ENST00000396946.8:c.1143+10C>G	ENSP00000380150.4:n.1143+10C>G
ENST00000698637.1:n.1469+10C>G
ENST00000698654.1:n.1402+10C>G
ENST00000698662.1:n.1343+10C>G
XM_011515585.1:c.1143+10C>G	XP_011513887.1:n.1143+10C>G
XM_011515586.1:c.1143+10C>G	XP_011513888.1:n.1143+10C>G
XM_011515586.2:c.1143+10C>G	XP_011513888.1:n.1143+10C>G
XM_011515587.1:c.1143+10C>G	XP_011513889.1:n.1143+10C>G
XM_011515587.2:c.1143+10C>G	XP_011513889.1:n.1143+10C>G
XR_001744885.1:n.1542+10C>G