Canonical Allele Identifier: CA1683424388

Gene: CARD11

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.2944529C= , CM000669.2:g.2944529C=	GRCh38
NC_000007.13:g.2984163C= , CM000669.1:g.2984163C=	GRCh37
NC_000007.12:g.2950689C=	NCBI36
NG_027759.1:g.104347G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698637.1:n.693G=
ENST00000698654.1:n.626G=
ENST00000698662.1:n.567G=
ENST00000396946.9:c.367G= MANE Select	ENSP00000380150.4:p.Gly123=
ENST00000396946.8:c.367G=	ENSP00000380150.4:p.Gly123=
NM_032415.5:c.367G=	NP_115791.3:p.Gly123=
XM_011515585.1:c.367G=	XP_011513887.1:p.Gly123=
XM_011515586.1:c.367G=	XP_011513888.1:p.Gly123=
XM_011515587.1:c.367G=	XP_011513889.1:p.Gly123=
NM_001324281.1:c.367G=	NP_001311210.1:p.Gly123=
XM_011515586.2:c.367G=	XP_011513888.1:p.Gly123=
XM_011515587.2:c.367G=	XP_011513889.1:p.Gly123=
XR_001744885.1:n.766G=
NM_001324281.2:c.367G=	NP_001311210.1:p.Gly123=
NM_032415.6:c.367G=	NP_115791.3:p.Gly123=
NM_001324281.3:c.367G=	NP_001311210.1:p.Gly123=
NM_032415.7:c.367G= MANE Select	NP_115791.3:p.Gly123=