Canonical Allele Identifier: CA4132135

Gene: CARD11

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.2919581G>A , CM000669.2:g.2919581G>A	GRCh38
NC_000007.13:g.2959215G>A , CM000669.1:g.2959215G>A	GRCh37
NC_000007.12:g.2925741G>A	NCBI36
NG_027759.1:g.129295C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_032415.7:c.2301C>T MANE Select	NP_115791.3:p.Asp767=
ENST00000396946.9:c.2301C>T MANE Select	ENSP00000380150.4:p.Asp767=
NM_001324281.1:c.2301C>T	NP_001311210.1:p.Asp767=
NM_001324281.2:c.2301C>T	NP_001311210.1:p.Asp767=
NM_001324281.3:c.2301C>T	NP_001311210.1:p.Asp767=
NM_032415.5:c.2301C>T	NP_115791.3:p.Asp767=
NM_032415.6:c.2301C>T	NP_115791.3:p.Asp767=
ENST00000355508.3:c.714C>T	ENSP00000347695.3:p.Asp238=
ENST00000396946.8:c.2301C>T	ENSP00000380150.4:p.Asp767=
ENST00000480332.1:n.439C>T
ENST00000698637.1:n.2627C>T
ENST00000698652.1:n.473C>T
XM_011515585.1:c.2301C>T	XP_011513887.1:p.Asp767=
XM_011515586.1:c.2301C>T	XP_011513888.1:p.Asp767=
XM_011515586.2:c.2301C>T	XP_011513888.1:p.Asp767=
XM_011515587.1:c.2298C>T	XP_011513889.1:p.Asp766=
XM_011515587.2:c.2298C>T	XP_011513889.1:p.Asp766=
XR_001744885.1:n.3045C>T