Canonical Allele Identifier: CA366642599

Gene: CARD11

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.2919461C>A , CM000669.2:g.2919461C>A	GRCh38
NC_000007.13:g.2959095C>A , CM000669.1:g.2959095C>A	GRCh37
NC_000007.12:g.2925621C>A	NCBI36
NG_027759.1:g.129415G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698637.1:n.2747G>T
ENST00000698652.1:n.593G>T
ENST00000396946.9:c.2421G>T MANE Select	ENSP00000380150.4:p.Met807Ile
ENST00000396946.8:c.2421G>T	ENSP00000380150.4:p.Met807Ile
ENST00000480332.1:n.559G>T
NM_032415.5:c.2421G>T	NP_115791.3:p.Met807Ile
XM_011515585.1:c.2421G>T	XP_011513887.1:p.Met807Ile
XM_011515586.1:c.2421G>T	XP_011513888.1:p.Met807Ile
XM_011515587.1:c.2418G>T	XP_011513889.1:p.Met806Ile
NM_001324281.1:c.2421G>T	NP_001311210.1:p.Met807Ile
XM_011515586.2:c.2421G>T	XP_011513888.1:p.Met807Ile
XM_011515587.2:c.2418G>T	XP_011513889.1:p.Met806Ile
XR_001744885.1:n.3165G>T
NM_001324281.2:c.2421G>T	NP_001311210.1:p.Met807Ile
NM_032415.6:c.2421G>T	NP_115791.3:p.Met807Ile
NM_001324281.3:c.2421G>T	NP_001311210.1:p.Met807Ile
NM_032415.7:c.2421G>T MANE Select	NP_115791.3:p.Met807Ile