Canonical Allele Identifier: CA4131723

Gene: CARD11

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.2906634C>T , CM000669.2:g.2906634C>T	GRCh38
NC_000007.13:g.2946268C>T , CM000669.1:g.2946268C>T	GRCh37
NC_000007.12:g.2912794C>T	NCBI36
NG_027759.1:g.142242G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_032415.7:c.*4G>A MANE Select	NP_115791.3:n.*4G>A
ENST00000396946.9:c.*4G>A MANE Select	ENSP00000380150.4:n.*4G>A
NM_001324281.1:c.*4G>A	NP_001311210.1:n.*4G>A
NM_001324281.2:c.*4G>A	NP_001311210.1:n.*4G>A
NM_001324281.3:c.*4G>A	NP_001311210.1:n.*4G>A
NM_032415.5:c.*4G>A	NP_115791.3:n.*4G>A
NM_032415.6:c.*4G>A	NP_115791.3:n.*4G>A
ENST00000396946.8:c.*4G>A	ENSP00000380150.4:n.*4G>A
ENST00000698637.1:n.4579G>A
ENST00000698652.1:n.2425G>A
XM_011515585.1:c.*4G>A	XP_011513887.1:n.*4G>A
XM_011515586.1:c.*4G>A	XP_011513888.1:n.*4G>A
XM_011515586.2:c.*4G>A	XP_011513888.1:n.*4G>A
XM_011515587.1:c.*4G>A	XP_011513889.1:n.*4G>A
XM_011515587.2:c.*4G>A	XP_011513889.1:n.*4G>A