Canonical Allele Identifier: CA4132430

Gene: CARD11

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.2930039G>C , CM000669.2:g.2930039G>C	GRCh38
NC_000007.13:g.2969673G>C , CM000669.1:g.2969673G>C	GRCh37
NC_000007.12:g.2936199G>C	NCBI36
NG_027759.1:g.118837C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_032415.7:c.1606C>G MANE Select	NP_115791.3:p.Pro536Ala
ENST00000396946.9:c.1606C>G MANE Select	ENSP00000380150.4:p.Pro536Ala
NM_001324281.1:c.1606C>G	NP_001311210.1:p.Pro536Ala
NM_001324281.2:c.1606C>G	NP_001311210.1:p.Pro536Ala
NM_001324281.3:c.1606C>G	NP_001311210.1:p.Pro536Ala
NM_032415.5:c.1606C>G	NP_115791.3:p.Pro536Ala
NM_032415.6:c.1606C>G	NP_115791.3:p.Pro536Ala
ENST00000355508.3:c.22C>G	ENSP00000347695.3:p.Pro8Ala
ENST00000396946.8:c.1606C>G	ENSP00000380150.4:p.Pro536Ala
ENST00000698637.1:n.1932C>G
XM_011515585.1:c.1606C>G	XP_011513887.1:p.Pro536Ala
XM_011515586.1:c.1606C>G	XP_011513888.1:p.Pro536Ala
XM_011515586.2:c.1606C>G	XP_011513888.1:p.Pro536Ala
XM_011515587.1:c.1606C>G	XP_011513889.1:p.Pro536Ala
XM_011515587.2:c.1606C>G	XP_011513889.1:p.Pro536Ala
XR_001744885.1:n.2005C>G