Canonical Allele Identifier: CA366647967

Gene: CARD11

Linked Data

• ClinVar Variation Id: 473938
• ClinVar RCV Id: RCV000528697 ; RCV000788795 ; RCV002285361
• dbSNP Id: rs145474800
• MyVariant Identifiers: chr7:g.2987341G>A (hg19) ; chr7:g.2947707G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.2947707G>A , CM000669.2:g.2947707G>A	GRCh38
NC_000007.13:g.2987341G>A , CM000669.1:g.2987341G>A	GRCh37
NC_000007.12:g.2953867G>A	NCBI36
NG_027759.1:g.101169C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698637.1:n.414C>T
ENST00000698654.1:n.313C>T
ENST00000698662.1:n.288C>T
ENST00000396946.9:c.88C>T MANE Select	ENSP00000380150.4:p.Arg30Trp
ENST00000356408.3:c.88C>T	ENSP00000348779.3:p.Arg30Trp
ENST00000396946.8:c.88C>T	ENSP00000380150.4:p.Arg30Trp
NM_032415.5:c.88C>T	NP_115791.3:p.Arg30Trp
XM_011515585.1:c.88C>T	XP_011513887.1:p.Arg30Trp
XM_011515586.1:c.88C>T	XP_011513888.1:p.Arg30Trp
XM_011515587.1:c.88C>T	XP_011513889.1:p.Arg30Trp
NM_001324281.1:c.88C>T	NP_001311210.1:p.Arg30Trp
XM_011515586.2:c.88C>T	XP_011513888.1:p.Arg30Trp
XM_011515587.2:c.88C>T	XP_011513889.1:p.Arg30Trp
XR_001744885.1:n.487C>T
NM_001324281.2:c.88C>T	NP_001311210.1:p.Arg30Trp
NM_032415.6:c.88C>T	NP_115791.3:p.Arg30Trp
NM_001324281.3:c.88C>T	NP_001311210.1:p.Arg30Trp
NM_032415.7:c.88C>T MANE Select	NP_115791.3:p.Arg30Trp