Canonical Allele Identifier: CA4132797

Gene: CARD11

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.2944385C>T , CM000669.2:g.2944385C>T	GRCh38
NC_000007.13:g.2984019C>T , CM000669.1:g.2984019C>T	GRCh37
NC_000007.12:g.2950545C>T	NCBI36
NG_027759.1:g.104491G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_032415.7:c.511G>A MANE Select	NP_115791.3:p.Val171Met
ENST00000396946.9:c.511G>A MANE Select	ENSP00000380150.4:p.Val171Met
NM_001324281.1:c.511G>A	NP_001311210.1:p.Val171Met
NM_001324281.2:c.511G>A	NP_001311210.1:p.Val171Met
NM_001324281.3:c.511G>A	NP_001311210.1:p.Val171Met
NM_032415.5:c.511G>A	NP_115791.3:p.Val171Met
NM_032415.6:c.511G>A	NP_115791.3:p.Val171Met
ENST00000396946.8:c.511G>A	ENSP00000380150.4:p.Val171Met
ENST00000698637.1:n.837G>A
ENST00000698654.1:n.770G>A
ENST00000698662.1:n.711G>A
XM_011515585.1:c.511G>A	XP_011513887.1:p.Val171Met
XM_011515586.1:c.511G>A	XP_011513888.1:p.Val171Met
XM_011515586.2:c.511G>A	XP_011513888.1:p.Val171Met
XM_011515587.1:c.511G>A	XP_011513889.1:p.Val171Met
XM_011515587.2:c.511G>A	XP_011513889.1:p.Val171Met
XR_001744885.1:n.910G>A