Canonical Allele Identifier: CA1683429114

Gene: CARD11

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.2947649C= , CM000669.2:g.2947649C=	GRCh38
NC_000007.13:g.2987283C= , CM000669.1:g.2987283C=	GRCh37
NC_000007.12:g.2953809C=	NCBI36
NG_027759.1:g.101227G=

Transcript Alleles

HGVS	Amino-acid Change
NM_032415.7:c.146G= MANE Select	NP_115791.3:p.Cys49=
ENST00000396946.9:c.146G= MANE Select	ENSP00000380150.4:p.Cys49=
NM_001324281.1:c.146G=	NP_001311210.1:p.Cys49=
NM_001324281.2:c.146G=	NP_001311210.1:p.Cys49=
NM_001324281.3:c.146G=	NP_001311210.1:p.Cys49=
NM_032415.5:c.146G=	NP_115791.3:p.Cys49=
NM_032415.6:c.146G=	NP_115791.3:p.Cys49=
ENST00000356408.3:c.146G=	ENSP00000348779.3:p.Cys49=
ENST00000396946.8:c.146G=	ENSP00000380150.4:p.Cys49=
ENST00000698637.1:n.472G=
ENST00000698654.1:n.371G=
ENST00000698662.1:n.346G=
XM_011515585.1:c.146G=	XP_011513887.1:p.Cys49=
XM_011515586.1:c.146G=	XP_011513888.1:p.Cys49=
XM_011515586.2:c.146G=	XP_011513888.1:p.Cys49=
XM_011515587.1:c.146G=	XP_011513889.1:p.Cys49=
XM_011515587.2:c.146G=	XP_011513889.1:p.Cys49=
XR_001744885.1:n.545G=