Canonical Allele Identifier: CA4131919

Gene: CARD11

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.2913359C>T , CM000669.2:g.2913359C>T	GRCh38
NC_000007.13:g.2952993C>T , CM000669.1:g.2952993C>T	GRCh37
NC_000007.12:g.2919519C>T	NCBI36
NG_027759.1:g.135517G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_032415.7:c.2947G>A MANE Select	NP_115791.3:p.Val983Met
ENST00000396946.9:c.2947G>A MANE Select	ENSP00000380150.4:p.Val983Met
NM_001324281.1:c.2947G>A	NP_001311210.1:p.Val983Met
NM_001324281.2:c.2947G>A	NP_001311210.1:p.Val983Met
NM_001324281.3:c.2947G>A	NP_001311210.1:p.Val983Met
NM_032415.5:c.2947G>A	NP_115791.3:p.Val983Met
NM_032415.6:c.2947G>A	NP_115791.3:p.Val983Met
ENST00000396946.8:c.2947G>A	ENSP00000380150.4:p.Val983Met
ENST00000698637.1:n.4057G>A
ENST00000698652.1:n.1903G>A
XM_011515585.1:c.2947G>A	XP_011513887.1:p.Val983Met
XM_011515586.1:c.2947G>A	XP_011513888.1:p.Val983Met
XM_011515586.2:c.2947G>A	XP_011513888.1:p.Val983Met
XM_011515587.1:c.2944G>A	XP_011513889.1:p.Val982Met
XM_011515587.2:c.2944G>A	XP_011513889.1:p.Val982Met