Canonical Allele Identifier: CA4131941

Gene: CARD11

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.2913437T>C , CM000669.2:g.2913437T>C	GRCh38
NC_000007.13:g.2953071T>C , CM000669.1:g.2953071T>C	GRCh37
NC_000007.12:g.2919597T>C	NCBI36
NG_027759.1:g.135439A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_032415.7:c.2869A>G MANE Select	NP_115791.3:p.Asn957Asp
ENST00000396946.9:c.2869A>G MANE Select	ENSP00000380150.4:p.Asn957Asp
NM_001324281.1:c.2869A>G	NP_001311210.1:p.Asn957Asp
NM_001324281.2:c.2869A>G	NP_001311210.1:p.Asn957Asp
NM_001324281.3:c.2869A>G	NP_001311210.1:p.Asn957Asp
NM_032415.5:c.2869A>G	NP_115791.3:p.Asn957Asp
NM_032415.6:c.2869A>G	NP_115791.3:p.Asn957Asp
ENST00000396946.8:c.2869A>G	ENSP00000380150.4:p.Asn957Asp
ENST00000698637.1:n.3979A>G
ENST00000698652.1:n.1825A>G
XM_011515585.1:c.2869A>G	XP_011513887.1:p.Asn957Asp
XM_011515586.1:c.2869A>G	XP_011513888.1:p.Asn957Asp
XM_011515586.2:c.2869A>G	XP_011513888.1:p.Asn957Asp
XM_011515587.1:c.2866A>G	XP_011513889.1:p.Asn956Asp
XM_011515587.2:c.2866A>G	XP_011513889.1:p.Asn956Asp