Canonical Allele Identifier: CA366646147

Gene: CARD11

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.2939748C>G , CM000669.2:g.2939748C>G	GRCh38
NC_000007.13:g.2979382C>G , CM000669.1:g.2979382C>G	GRCh37
NC_000007.12:g.2945908C>G	NCBI36
NG_027759.1:g.109128G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_032415.7:c.864+1G>C MANE Select	NP_115791.3:n.864+1G>C
ENST00000396946.9:c.864+1G>C MANE Select	ENSP00000380150.4:n.864+1G>C
NM_001324281.1:c.864+1G>C	NP_001311210.1:n.864+1G>C
NM_001324281.2:c.864+1G>C	NP_001311210.1:n.864+1G>C
NM_001324281.3:c.864+1G>C	NP_001311210.1:n.864+1G>C
NM_032415.5:c.864+1G>C	NP_115791.3:n.864+1G>C
NM_032415.6:c.864+1G>C	NP_115791.3:n.864+1G>C
ENST00000396946.8:c.864+1G>C	ENSP00000380150.4:n.864+1G>C
ENST00000698637.1:n.1190+1G>C
ENST00000698654.1:n.1123+1G>C
ENST00000698662.1:n.1064+1G>C
XM_011515585.1:c.864+1G>C	XP_011513887.1:n.864+1G>C
XM_011515586.1:c.864+1G>C	XP_011513888.1:n.864+1G>C
XM_011515586.2:c.864+1G>C	XP_011513888.1:n.864+1G>C
XM_011515587.1:c.864+1G>C	XP_011513889.1:n.864+1G>C
XM_011515587.2:c.864+1G>C	XP_011513889.1:n.864+1G>C
XR_001744885.1:n.1263+1G>C