Canonical Allele Identifier: CA4131926

Gene: CARD11

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.2913386G>A , CM000669.2:g.2913386G>A	GRCh38
NC_000007.13:g.2953020G>A , CM000669.1:g.2953020G>A	GRCh37
NC_000007.12:g.2919546G>A	NCBI36
NG_027759.1:g.135490C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_032415.7:c.2920C>T MANE Select	NP_115791.3:p.Arg974Cys
ENST00000396946.9:c.2920C>T MANE Select	ENSP00000380150.4:p.Arg974Cys
NM_001324281.1:c.2920C>T	NP_001311210.1:p.Arg974Cys
NM_001324281.2:c.2920C>T	NP_001311210.1:p.Arg974Cys
NM_001324281.3:c.2920C>T	NP_001311210.1:p.Arg974Cys
NM_032415.5:c.2920C>T	NP_115791.3:p.Arg974Cys
NM_032415.6:c.2920C>T	NP_115791.3:p.Arg974Cys
ENST00000396946.8:c.2920C>T	ENSP00000380150.4:p.Arg974Cys
ENST00000698637.1:n.4030C>T
ENST00000698652.1:n.1876C>T
XM_011515585.1:c.2920C>T	XP_011513887.1:p.Arg974Cys
XM_011515586.1:c.2920C>T	XP_011513888.1:p.Arg974Cys
XM_011515586.2:c.2920C>T	XP_011513888.1:p.Arg974Cys
XM_011515587.1:c.2917C>T	XP_011513889.1:p.Arg973Cys
XM_011515587.2:c.2917C>T	XP_011513889.1:p.Arg973Cys