Canonical Allele Identifier: CA366646403

Gene: CARD11

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.2939861A>G , CM000669.2:g.2939861A>G	GRCh38
NC_000007.13:g.2979495A>G , CM000669.1:g.2979495A>G	GRCh37
NC_000007.12:g.2946021A>G	NCBI36
NG_027759.1:g.109015T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_032415.7:c.752T>C MANE Select	NP_115791.3:p.Leu251Pro
ENST00000396946.9:c.752T>C MANE Select	ENSP00000380150.4:p.Leu251Pro
NM_001324281.1:c.752T>C	NP_001311210.1:p.Leu251Pro
NM_001324281.2:c.752T>C	NP_001311210.1:p.Leu251Pro
NM_001324281.3:c.752T>C	NP_001311210.1:p.Leu251Pro
NM_032415.5:c.752T>C	NP_115791.3:p.Leu251Pro
NM_032415.6:c.752T>C	NP_115791.3:p.Leu251Pro
ENST00000396946.8:c.752T>C	ENSP00000380150.4:p.Leu251Pro
ENST00000698637.1:n.1078T>C
ENST00000698654.1:n.1011T>C
ENST00000698662.1:n.952T>C
XM_011515585.1:c.752T>C	XP_011513887.1:p.Leu251Pro
XM_011515586.1:c.752T>C	XP_011513888.1:p.Leu251Pro
XM_011515586.2:c.752T>C	XP_011513888.1:p.Leu251Pro
XM_011515587.1:c.752T>C	XP_011513889.1:p.Leu251Pro
XM_011515587.2:c.752T>C	XP_011513889.1:p.Leu251Pro
XR_001744885.1:n.1151T>C