Canonical Allele Identifier: CA16618451

Gene: CARD11 CARD11-AS1

Linked Data

• ClinVar Variation Id: 421663
• ClinVar RCV Id: RCV000726904 ; RCV002526603
• dbSNP Id: rs1064795280
• gnomAD v4: 7-2945953-C-T
• MyVariant Identifiers: chr7:g.2985587C>T (hg19) ; chr7:g.2945953C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.2945953C>T , CM000669.2:g.2945953C>T	GRCh38
NC_000007.13:g.2985587C>T , CM000669.1:g.2985587C>T	GRCh37
NC_000007.12:g.2952113C>T	NCBI36
NG_027759.1:g.102923G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698637.1:n.550G>A (CARD11)
ENST00000698654.1:n.449G>A (CARD11)
ENST00000698662.1:n.424G>A (CARD11)
ENST00000396946.9:c.224G>A (CARD11) MANE Select	ENSP00000380150.4:p.Arg75Gln
ENST00000396946.8:c.224G>A (CARD11)	ENSP00000380150.4:p.Arg75Gln
NM_032415.5:c.224G>A (CARD11)	NP_115791.3:p.Arg75Gln
XM_011515585.1:c.224G>A (CARD11)	XP_011513887.1:p.Arg75Gln
XM_011515586.1:c.224G>A (CARD11)	XP_011513888.1:p.Arg75Gln
XM_011515587.1:c.224G>A (CARD11)	XP_011513889.1:p.Arg75Gln
XR_926993.1:n.57-644C>T (CARD11-AS1)
NM_001324281.1:c.224G>A (CARD11)	NP_001311210.1:p.Arg75Gln
XM_011515586.2:c.224G>A (CARD11)	XP_011513888.1:p.Arg75Gln
XM_011515587.2:c.224G>A (CARD11)	XP_011513889.1:p.Arg75Gln
XR_001744885.1:n.623G>A (CARD11)
NM_001324281.2:c.224G>A (CARD11)	NP_001311210.1:p.Arg75Gln
NM_032415.6:c.224G>A (CARD11)	NP_115791.3:p.Arg75Gln
NM_001324281.3:c.224G>A (CARD11)	NP_001311210.1:p.Arg75Gln
NM_032415.7:c.224G>A (CARD11) MANE Select	NP_115791.3:p.Arg75Gln