Canonical Allele Identifier: CA4132344

Gene: CARD11

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.2926811T>G , CM000669.2:g.2926811T>G	GRCh38
NC_000007.13:g.2966445T>G , CM000669.1:g.2966445T>G	GRCh37
NC_000007.12:g.2932971T>G	NCBI36
NG_027759.1:g.122065A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_032415.7:c.1755-20A>C MANE Select	NP_115791.3:n.1755-20A>C
ENST00000396946.9:c.1755-20A>C MANE Select	ENSP00000380150.4:n.1755-20A>C
NM_001324281.1:c.1755-20A>C	NP_001311210.1:n.1755-20A>C
NM_001324281.2:c.1755-20A>C	NP_001311210.1:n.1755-20A>C
NM_001324281.3:c.1755-20A>C	NP_001311210.1:n.1755-20A>C
NM_032415.5:c.1755-20A>C	NP_115791.3:n.1755-20A>C
NM_032415.6:c.1755-20A>C	NP_115791.3:n.1755-20A>C
ENST00000355508.3:c.168-20A>C	ENSP00000347695.3:n.168-20A>C
ENST00000396946.8:c.1755-20A>C	ENSP00000380150.4:n.1755-20A>C
ENST00000698637.1:n.2081-20A>C
XM_011515585.1:c.1755-20A>C	XP_011513887.1:n.1755-20A>C
XM_011515586.1:c.1755-20A>C	XP_011513888.1:n.1755-20A>C
XM_011515586.2:c.1755-20A>C	XP_011513888.1:n.1755-20A>C
XM_011515587.1:c.1752-20A>C	XP_011513889.1:n.1752-20A>C
XM_011515587.2:c.1752-20A>C	XP_011513889.1:n.1752-20A>C
XR_001744885.1:n.2154-20A>C