Canonical Allele Identifier: CA366641180

Gene: CARD11

Linked Data

• MyVariant Identifiers: chr7:g.2951887C>A (hg19) ; chr7:g.2912253C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.2912253C>A , CM000669.2:g.2912253C>A	GRCh38
NC_000007.13:g.2951887C>A , CM000669.1:g.2951887C>A	GRCh37
NC_000007.12:g.2918413C>A	NCBI36
NG_027759.1:g.136623G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698637.1:n.4173G>T
ENST00000698652.1:n.2019G>T
ENST00000396946.9:c.3063G>T MANE Select	ENSP00000380150.4:p.Glu1021Asp
ENST00000396946.8:c.3063G>T	ENSP00000380150.4:p.Glu1021Asp
NM_032415.5:c.3063G>T	NP_115791.3:p.Glu1021Asp
XM_011515585.1:c.3063G>T	XP_011513887.1:p.Glu1021Asp
XM_011515586.1:c.3063G>T	XP_011513888.1:p.Glu1021Asp
XM_011515587.1:c.3060G>T	XP_011513889.1:p.Glu1020Asp
NM_001324281.1:c.3063G>T	NP_001311210.1:p.Glu1021Asp
XM_011515586.2:c.3063G>T	XP_011513888.1:p.Glu1021Asp
XM_011515587.2:c.3060G>T	XP_011513889.1:p.Glu1020Asp
NM_001324281.2:c.3063G>T	NP_001311210.1:p.Glu1021Asp
NM_032415.6:c.3063G>T	NP_115791.3:p.Glu1021Asp
NM_001324281.3:c.3063G>T	NP_001311210.1:p.Glu1021Asp
NM_032415.7:c.3063G>T MANE Select	NP_115791.3:p.Glu1021Asp