Canonical Allele Identifier: CA366647646

Gene: CARD11 CARD11-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.2945954G>A , CM000669.2:g.2945954G>A	GRCh38
NC_000007.13:g.2985588G>A , CM000669.1:g.2985588G>A	GRCh37
NC_000007.12:g.2952114G>A	NCBI36
NG_027759.1:g.102922C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_032415.7:c.223C>T (CARD11) MANE Select	NP_115791.3:p.Arg75Trp
ENST00000396946.9:c.223C>T (CARD11) MANE Select	ENSP00000380150.4:p.Arg75Trp
NM_001324281.1:c.223C>T (CARD11)	NP_001311210.1:p.Arg75Trp
NM_001324281.2:c.223C>T (CARD11)	NP_001311210.1:p.Arg75Trp
NM_001324281.3:c.223C>T (CARD11)	NP_001311210.1:p.Arg75Trp
NM_032415.5:c.223C>T (CARD11)	NP_115791.3:p.Arg75Trp
NM_032415.6:c.223C>T (CARD11)	NP_115791.3:p.Arg75Trp
ENST00000396946.8:c.223C>T (CARD11)	ENSP00000380150.4:p.Arg75Trp
ENST00000698637.1:n.549C>T (CARD11)
ENST00000698654.1:n.448C>T (CARD11)
ENST00000698662.1:n.423C>T (CARD11)
XM_011515585.1:c.223C>T (CARD11)	XP_011513887.1:p.Arg75Trp
XM_011515586.1:c.223C>T (CARD11)	XP_011513888.1:p.Arg75Trp
XM_011515586.2:c.223C>T (CARD11)	XP_011513888.1:p.Arg75Trp
XM_011515587.1:c.223C>T (CARD11)	XP_011513889.1:p.Arg75Trp
XM_011515587.2:c.223C>T (CARD11)	XP_011513889.1:p.Arg75Trp
XR_001744885.1:n.622C>T (CARD11)
XR_926993.1:n.57-643G>A (CARD11-AS1)