Canonical Allele Identifier: CA1683442089
Community Standard Title: NM_032415.7(CARD11):c.1341+15G>A
Gene: CARD11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.2937022C>T , CM000669.2:g.2937022C>T GRCh38
NC_000007.13:g.2976656C>T , CM000669.1:g.2976656C>T GRCh37
NC_000007.12:g.2943182C>T NCBI36
NG_027759.1:g.111854G>A

Transcript Alleles

HGVS Amino-acid Change
NM_032415.7:c.1341+15G>A MANE Select NP_115791.3:n.1341+15G>A
ENST00000396946.9:c.1341+15G>A MANE Select ENSP00000380150.4:n.1341+15G>A
NM_001324281.1:c.1341+15G>A NP_001311210.1:n.1341+15G>A
NM_001324281.2:c.1341+15G>A NP_001311210.1:n.1341+15G>A
NM_001324281.3:c.1341+15G>A NP_001311210.1:n.1341+15G>A
NM_032415.5:c.1341+15G>A NP_115791.3:n.1341+15G>A
NM_032415.6:c.1341+15G>A NP_115791.3:n.1341+15G>A
ENST00000396946.8:c.1341+15G>A ENSP00000380150.4:n.1341+15G>A
ENST00000698637.1:n.1667+15G>A
ENST00000698654.1:n.1600+15G>A
ENST00000698662.1:n.1541+15G>A
XM_011515585.1:c.1341+15G>A XP_011513887.1:n.1341+15G>A
XM_011515586.1:c.1341+15G>A XP_011513888.1:n.1341+15G>A
XM_011515586.2:c.1341+15G>A XP_011513888.1:n.1341+15G>A
XM_011515587.1:c.1341+15G>A XP_011513889.1:n.1341+15G>A
XM_011515587.2:c.1341+15G>A XP_011513889.1:n.1341+15G>A
XR_001744885.1:n.1740+15G>A