Canonical Allele Identifier: CA366647661

Gene: CARD11

Linked Data

• ClinVar Variation Id: 489270
• ClinVar RCV Id: RCV000579340 ; RCV001543392 ; RCV003767257
• dbSNP Id: rs1554276623
• MyVariant Identifiers: chr7:g.2987208C>T (hg19) ; chr7:g.2947574C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.2947574C>T , CM000669.2:g.2947574C>T	GRCh38
NC_000007.13:g.2987208C>T , CM000669.1:g.2987208C>T	GRCh37
NC_000007.12:g.2953734C>T	NCBI36
NG_027759.1:g.101302G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698637.1:n.546+1G>A
ENST00000698654.1:n.445+1G>A
ENST00000698662.1:n.420+1G>A
ENST00000396946.9:c.220+1G>A MANE Select	ENSP00000380150.4:n.220+1G>A
ENST00000396946.8:c.220+1G>A	ENSP00000380150.4:n.220+1G>A
NM_032415.5:c.220+1G>A	NP_115791.3:n.220+1G>A
XM_011515585.1:c.220+1G>A	XP_011513887.1:n.220+1G>A
XM_011515586.1:c.220+1G>A	XP_011513888.1:n.220+1G>A
XM_011515587.1:c.220+1G>A	XP_011513889.1:n.220+1G>A
NM_001324281.1:c.220+1G>A	NP_001311210.1:n.220+1G>A
XM_011515586.2:c.220+1G>A	XP_011513888.1:n.220+1G>A
XM_011515587.2:c.220+1G>A	XP_011513889.1:n.220+1G>A
XR_001744885.1:n.619+1G>A
NM_001324281.2:c.220+1G>A	NP_001311210.1:n.220+1G>A
NM_032415.6:c.220+1G>A	NP_115791.3:n.220+1G>A
NM_001324281.3:c.220+1G>A	NP_001311210.1:n.220+1G>A
NM_032415.7:c.220+1G>A MANE Select	NP_115791.3:n.220+1G>A