Canonical Allele Identifier: CA366640273

Gene: CARD11

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.2958499C>G , CM000669.2:g.2958499C>G	GRCh38
NC_000007.13:g.2998133C>G , CM000669.1:g.2998133C>G	GRCh37
NC_000007.12:g.2964659C>G	NCBI36
NG_027759.1:g.90377G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_032415.7:c.7+1G>C MANE Select	NP_115791.3:n.7+1G>C
ENST00000396946.9:c.7+1G>C MANE Select	ENSP00000380150.4:n.7+1G>C
NM_001324281.1:c.7+1G>C	NP_001311210.1:n.7+1G>C
NM_001324281.2:c.7+1G>C	NP_001311210.1:n.7+1G>C
NM_001324281.3:c.7+1G>C	NP_001311210.1:n.7+1G>C
NM_032415.5:c.7+1G>C	NP_115791.3:n.7+1G>C
NM_032415.6:c.7+1G>C	NP_115791.3:n.7+1G>C
ENST00000356408.3:c.7+1G>C	ENSP00000348779.3:n.7+1G>C
ENST00000396946.8:c.7+1G>C	ENSP00000380150.4:n.7+1G>C
ENST00000698637.1:n.333+1G>C
ENST00000698654.1:n.232+1G>C
ENST00000698662.1:n.207+1G>C
XM_011515585.1:c.7+1G>C	XP_011513887.1:n.7+1G>C
XM_011515586.1:c.7+1G>C	XP_011513888.1:n.7+1G>C
XM_011515586.2:c.7+1G>C	XP_011513888.1:n.7+1G>C
XM_011515587.1:c.7+1G>C	XP_011513889.1:n.7+1G>C
XM_011515587.2:c.7+1G>C	XP_011513889.1:n.7+1G>C
XR_001744885.1:n.406+1G>C