Canonical Allele Identifier: CA366642559

Gene: CARD11

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.2919445C>A , CM000669.2:g.2919445C>A	GRCh38
NC_000007.13:g.2959079C>A , CM000669.1:g.2959079C>A	GRCh37
NC_000007.12:g.2925605C>A	NCBI36
NG_027759.1:g.129431G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_032415.7:c.2437G>T MANE Select	NP_115791.3:p.Glu813Ter
ENST00000396946.9:c.2437G>T MANE Select	ENSP00000380150.4:p.Glu813Ter
NM_001324281.1:c.2437G>T	NP_001311210.1:p.Glu813Ter
NM_001324281.2:c.2437G>T	NP_001311210.1:p.Glu813Ter
NM_001324281.3:c.2437G>T	NP_001311210.1:p.Glu813Ter
NM_032415.5:c.2437G>T	NP_115791.3:p.Glu813Ter
NM_032415.6:c.2437G>T	NP_115791.3:p.Glu813Ter
ENST00000396946.8:c.2437G>T	ENSP00000380150.4:p.Glu813Ter
ENST00000480332.1:n.575G>T
ENST00000698637.1:n.2763G>T
ENST00000698652.1:n.609G>T
XM_011515585.1:c.2437G>T	XP_011513887.1:p.Glu813Ter
XM_011515586.1:c.2437G>T	XP_011513888.1:p.Glu813Ter
XM_011515586.2:c.2437G>T	XP_011513888.1:p.Glu813Ter
XM_011515587.1:c.2434G>T	XP_011513889.1:p.Glu812Ter
XM_011515587.2:c.2434G>T	XP_011513889.1:p.Glu812Ter
XR_001744885.1:n.3181G>T