Canonical Allele Identifier: CA1683424385

Gene: CARD11

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.2944528C= , CM000669.2:g.2944528C=	GRCh38
NC_000007.13:g.2984162C= , CM000669.1:g.2984162C=	GRCh37
NC_000007.12:g.2950688C=	NCBI36
NG_027759.1:g.104348G=

Transcript Alleles

HGVS	Amino-acid Change
NM_032415.7:c.368G= MANE Select	NP_115791.3:p.Gly123=
ENST00000396946.9:c.368G= MANE Select	ENSP00000380150.4:p.Gly123=
NM_001324281.1:c.368G=	NP_001311210.1:p.Gly123=
NM_001324281.2:c.368G=	NP_001311210.1:p.Gly123=
NM_001324281.3:c.368G=	NP_001311210.1:p.Gly123=
NM_032415.5:c.368G=	NP_115791.3:p.Gly123=
NM_032415.6:c.368G=	NP_115791.3:p.Gly123=
ENST00000396946.8:c.368G=	ENSP00000380150.4:p.Gly123=
ENST00000698637.1:n.694G=
ENST00000698654.1:n.627G=
ENST00000698662.1:n.568G=
XM_011515585.1:c.368G=	XP_011513887.1:p.Gly123=
XM_011515586.1:c.368G=	XP_011513888.1:p.Gly123=
XM_011515586.2:c.368G=	XP_011513888.1:p.Gly123=
XM_011515587.1:c.368G=	XP_011513889.1:p.Gly123=
XM_011515587.2:c.368G=	XP_011513889.1:p.Gly123=
XR_001744885.1:n.767G=