Canonical Allele Identifier: CA2580076712

Gene: CARD11

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.2906826_2906827delinsAC , CM000669.2:g.2906826_2906827delinsAC	GRCh38
NC_000007.13:g.2946460_2946461delinsAC , CM000669.1:g.2946460_2946461delinsAC	GRCh37
NC_000007.12:g.2912986_2912987delinsAC	NCBI36
NG_027759.1:g.142049_142050delinsGT

Transcript Alleles

HGVS	Amino-acid Change
NM_032415.7:c.3276_3277delinsGT MANE Select	NP_115791.3:p.Pro1093Ser
ENST00000396946.9:c.3276_3277delinsGT MANE Select	ENSP00000380150.4:p.Pro1093Ser
NM_001324281.1:c.3276_3277delinsGT	NP_001311210.1:p.Pro1093Ser
NM_001324281.2:c.3276_3277delinsGT	NP_001311210.1:p.Pro1093Ser
NM_001324281.3:c.3276_3277delinsGT	NP_001311210.1:p.Pro1093Ser
NM_032415.5:c.3276_3277delinsGT	NP_115791.3:p.Pro1093Ser
NM_032415.6:c.3276_3277delinsGT	NP_115791.3:p.Pro1093Ser
ENST00000396946.8:c.3276_3277delinsGT	ENSP00000380150.4:p.Pro1093Ser
ENST00000698637.1:n.4386_4387delinsGT
ENST00000698652.1:n.2232_2233delinsGT
XM_011515585.1:c.3276_3277delinsGT	XP_011513887.1:p.Pro1093Ser
XM_011515586.1:c.3276_3277delinsGT	XP_011513888.1:p.Pro1093Ser
XM_011515586.2:c.3276_3277delinsGT	XP_011513888.1:p.Pro1093Ser
XM_011515587.1:c.3273_3274delinsGT	XP_011513889.1:p.Pro1092Ser
XM_011515587.2:c.3273_3274delinsGT	XP_011513889.1:p.Pro1092Ser