Canonical Allele Identifier: CA366643650

Gene: CARD11

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.2924232C>A , CM000669.2:g.2924232C>A	GRCh38
NC_000007.13:g.2963866C>A , CM000669.1:g.2963866C>A	GRCh37
NC_000007.12:g.2930392C>A	NCBI36
NG_027759.1:g.124644G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_032415.7:c.1940+1G>T MANE Select	NP_115791.3:n.1940+1G>T
ENST00000396946.9:c.1940+1G>T MANE Select	ENSP00000380150.4:n.1940+1G>T
NM_001324281.1:c.1940+1G>T	NP_001311210.1:n.1940+1G>T
NM_001324281.2:c.1940+1G>T	NP_001311210.1:n.1940+1G>T
NM_001324281.3:c.1940+1G>T	NP_001311210.1:n.1940+1G>T
NM_032415.5:c.1940+1G>T	NP_115791.3:n.1940+1G>T
NM_032415.6:c.1940+1G>T	NP_115791.3:n.1940+1G>T
ENST00000355508.3:c.353+1G>T	ENSP00000347695.3:n.353+1G>T
ENST00000396946.8:c.1940+1G>T	ENSP00000380150.4:n.1940+1G>T
ENST00000698637.1:n.2266+1G>T
XM_011515585.1:c.1940+1G>T	XP_011513887.1:n.1940+1G>T
XM_011515586.1:c.1940+1G>T	XP_011513888.1:n.1940+1G>T
XM_011515586.2:c.1940+1G>T	XP_011513888.1:n.1940+1G>T
XM_011515587.1:c.1937+1G>T	XP_011513889.1:n.1937+1G>T
XM_011515587.2:c.1937+1G>T	XP_011513889.1:n.1937+1G>T
XR_001744885.1:n.2339+1G>T