Canonical Allele Identifier: CA4132816

Gene: CARD11

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.2944473C>A , CM000669.2:g.2944473C>A	GRCh38
NC_000007.13:g.2984107C>A , CM000669.1:g.2984107C>A	GRCh37
NC_000007.12:g.2950633C>A	NCBI36
NG_027759.1:g.104403G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698637.1:n.749G>T
ENST00000698654.1:n.682G>T
ENST00000698662.1:n.623G>T
ENST00000396946.9:c.423G>T MANE Select	ENSP00000380150.4:p.Gln141His
ENST00000396946.8:c.423G>T	ENSP00000380150.4:p.Gln141His
NM_032415.5:c.423G>T	NP_115791.3:p.Gln141His
XM_011515585.1:c.423G>T	XP_011513887.1:p.Gln141His
XM_011515586.1:c.423G>T	XP_011513888.1:p.Gln141His
XM_011515587.1:c.423G>T	XP_011513889.1:p.Gln141His
NM_001324281.1:c.423G>T	NP_001311210.1:p.Gln141His
XM_011515586.2:c.423G>T	XP_011513888.1:p.Gln141His
XM_011515587.2:c.423G>T	XP_011513889.1:p.Gln141His
XR_001744885.1:n.822G>T
NM_001324281.2:c.423G>T	NP_001311210.1:p.Gln141His
NM_032415.6:c.423G>T	NP_115791.3:p.Gln141His
NM_001324281.3:c.423G>T	NP_001311210.1:p.Gln141His
NM_032415.7:c.423G>T MANE Select	NP_115791.3:p.Gln141His