Canonical Allele Identifier: CA4132873

Gene: CARD11

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.2947559G>A , CM000669.2:g.2947559G>A	GRCh38
NC_000007.13:g.2987193G>A , CM000669.1:g.2987193G>A	GRCh37
NC_000007.12:g.2953719G>A	NCBI36
NG_027759.1:g.101317C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698637.1:n.546+16C>T
ENST00000698654.1:n.445+16C>T
ENST00000698662.1:n.420+16C>T
ENST00000396946.9:c.220+16C>T MANE Select	ENSP00000380150.4:n.220+16C>T
ENST00000396946.8:c.220+16C>T	ENSP00000380150.4:n.220+16C>T
NM_032415.5:c.220+16C>T	NP_115791.3:n.220+16C>T
XM_011515585.1:c.220+16C>T	XP_011513887.1:n.220+16C>T
XM_011515586.1:c.220+16C>T	XP_011513888.1:n.220+16C>T
XM_011515587.1:c.220+16C>T	XP_011513889.1:n.220+16C>T
NM_001324281.1:c.220+16C>T	NP_001311210.1:n.220+16C>T
XM_011515586.2:c.220+16C>T	XP_011513888.1:n.220+16C>T
XM_011515587.2:c.220+16C>T	XP_011513889.1:n.220+16C>T
XR_001744885.1:n.619+16C>T
NM_001324281.2:c.220+16C>T	NP_001311210.1:n.220+16C>T
NM_032415.6:c.220+16C>T	NP_115791.3:n.220+16C>T
NM_001324281.3:c.220+16C>T	NP_001311210.1:n.220+16C>T
NM_032415.7:c.220+16C>T MANE Select	NP_115791.3:n.220+16C>T