Canonical Allele Identifier: CA1683417769

Gene: CARD11

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.2915243G= , CM000669.2:g.2915243G=	GRCh38
NC_000007.13:g.2954877G= , CM000669.1:g.2954877G=	GRCh37
NC_000007.12:g.2921403G=	NCBI36
NG_027759.1:g.133633C=

Transcript Alleles

HGVS	Amino-acid Change
NM_032415.7:c.2833C= MANE Select	NP_115791.3:p.Gln945=
ENST00000396946.9:c.2833C= MANE Select	ENSP00000380150.4:p.Gln945=
NM_001324281.1:c.2833C=	NP_001311210.1:p.Gln945=
NM_001324281.2:c.2833C=	NP_001311210.1:p.Gln945=
NM_001324281.3:c.2833C=	NP_001311210.1:p.Gln945=
NM_032415.5:c.2833C=	NP_115791.3:p.Gln945=
NM_032415.6:c.2833C=	NP_115791.3:p.Gln945=
ENST00000396946.8:c.2833C=	ENSP00000380150.4:p.Gln945=
ENST00000698637.1:n.3943C=
ENST00000698652.1:n.1789C=
XM_011515585.1:c.2833C=	XP_011513887.1:p.Gln945=
XM_011515586.1:c.2833C=	XP_011513888.1:p.Gln945=
XM_011515586.2:c.2833C=	XP_011513888.1:p.Gln945=
XM_011515587.1:c.2830C=	XP_011513889.1:p.Gln944=
XM_011515587.2:c.2830C=	XP_011513889.1:p.Gln944=