Canonical Allele Identifier: CA4131760

Gene: CARD11

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.2906826G>A , CM000669.2:g.2906826G>A	GRCh38
NC_000007.13:g.2946460G>A , CM000669.1:g.2946460G>A	GRCh37
NC_000007.12:g.2912986G>A	NCBI36
NG_027759.1:g.142050C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_032415.7:c.3277C>T MANE Select	NP_115791.3:p.Pro1093Ser
ENST00000396946.9:c.3277C>T MANE Select	ENSP00000380150.4:p.Pro1093Ser
NM_001324281.1:c.3277C>T	NP_001311210.1:p.Pro1093Ser
NM_001324281.2:c.3277C>T	NP_001311210.1:p.Pro1093Ser
NM_001324281.3:c.3277C>T	NP_001311210.1:p.Pro1093Ser
NM_032415.5:c.3277C>T	NP_115791.3:p.Pro1093Ser
NM_032415.6:c.3277C>T	NP_115791.3:p.Pro1093Ser
ENST00000396946.8:c.3277C>T	ENSP00000380150.4:p.Pro1093Ser
ENST00000698637.1:n.4387C>T
ENST00000698652.1:n.2233C>T
XM_011515585.1:c.3277C>T	XP_011513887.1:p.Pro1093Ser
XM_011515586.1:c.3277C>T	XP_011513888.1:p.Pro1093Ser
XM_011515586.2:c.3277C>T	XP_011513888.1:p.Pro1093Ser
XM_011515587.1:c.3274C>T	XP_011513889.1:p.Pro1092Ser
XM_011515587.2:c.3274C>T	XP_011513889.1:p.Pro1092Ser