Canonical Allele Identifier: CA1683429077

Gene: CARD11

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.2947624T= , CM000669.2:g.2947624T=	GRCh38
NC_000007.13:g.2987258T= , CM000669.1:g.2987258T=	GRCh37
NC_000007.12:g.2953784T=	NCBI36
NG_027759.1:g.101252A=

Transcript Alleles

HGVS	Amino-acid Change
NM_032415.7:c.171A= MANE Select	NP_115791.3:p.Glu57=
ENST00000396946.9:c.171A= MANE Select	ENSP00000380150.4:p.Glu57=
NM_001324281.1:c.171A=	NP_001311210.1:p.Glu57=
NM_001324281.2:c.171A=	NP_001311210.1:p.Glu57=
NM_001324281.3:c.171A=	NP_001311210.1:p.Glu57=
NM_032415.5:c.171A=	NP_115791.3:p.Glu57=
NM_032415.6:c.171A=	NP_115791.3:p.Glu57=
ENST00000356408.3:c.171A=	ENSP00000348779.3:p.Glu57=
ENST00000396946.8:c.171A=	ENSP00000380150.4:p.Glu57=
ENST00000698637.1:n.497A=
ENST00000698654.1:n.396A=
ENST00000698662.1:n.371A=
XM_011515585.1:c.171A=	XP_011513887.1:p.Glu57=
XM_011515586.1:c.171A=	XP_011513888.1:p.Glu57=
XM_011515586.2:c.171A=	XP_011513888.1:p.Glu57=
XM_011515587.1:c.171A=	XP_011513889.1:p.Glu57=
XM_011515587.2:c.171A=	XP_011513889.1:p.Glu57=
XR_001744885.1:n.570A=