Canonical Allele Identifier: CA4132381

Gene: CARD11

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.2928657G>A , CM000669.2:g.2928657G>A	GRCh38
NC_000007.13:g.2968291G>A , CM000669.1:g.2968291G>A	GRCh37
NC_000007.12:g.2934817G>A	NCBI36
NG_027759.1:g.120219C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698637.1:n.2021C>T
ENST00000396946.9:c.1695C>T MANE Select	ENSP00000380150.4:p.Ala565=
ENST00000355508.3:c.108C>T	ENSP00000347695.3:p.Ala36=
ENST00000396946.8:c.1695C>T	ENSP00000380150.4:p.Ala565=
NM_032415.5:c.1695C>T	NP_115791.3:p.Ala565=
XM_011515585.1:c.1695C>T	XP_011513887.1:p.Ala565=
XM_011515586.1:c.1695C>T	XP_011513888.1:p.Ala565=
XM_011515587.1:c.1692C>T	XP_011513889.1:p.Ala564=
NM_001324281.1:c.1695C>T	NP_001311210.1:p.Ala565=
XM_011515586.2:c.1695C>T	XP_011513888.1:p.Ala565=
XM_011515587.2:c.1692C>T	XP_011513889.1:p.Ala564=
XR_001744885.1:n.2094C>T
NM_001324281.2:c.1695C>T	NP_001311210.1:p.Ala565=
NM_032415.6:c.1695C>T	NP_115791.3:p.Ala565=
NM_001324281.3:c.1695C>T	NP_001311210.1:p.Ala565=
NM_032415.7:c.1695C>T MANE Select	NP_115791.3:p.Ala565=