Canonical Allele Identifier: CA1884186532

Gene: CARD9

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136371857T= , CM000671.2:g.136371857T=	GRCh38
NC_000009.11:g.139266309T= , CM000671.1:g.139266309T=	GRCh37
NC_000009.10:g.138386130T=	NCBI36
NG_021197.1:g.6825A= , LRG_178:g.6825A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000641290.2:n.189+38A=
ENST00000695905.1:n.312+38A=
ENST00000695906.1:n.312+38A=
ENST00000695908.1:n.303+38A=
ENST00000696169.1:c.184+38A=	ENSP00000512460.1:n.184+38A=
ENST00000371732.10:c.184+38A= MANE Select	ENSP00000360797.5:n.184+38A=
ENST00000641290.1:c.-129+38A=	ENSP00000493113.1:n.-129+38A=
ENST00000371732.9:c.184+38A=	ENSP00000360797.5:n.184+38A=
ENST00000371734.7:c.184+38A=	ENSP00000360799.3:n.184+38A=
ENST00000481053.5:n.313+38A=
ENST00000489932.2:c.184+38A=	ENSP00000451368.1:n.184+38A=
ENST00000556340.1:n.315+38A=
NM_052813.4:c.184+38A= , LRG_178t1:c.184+38A=	NP_434700.2:n.184+38A=
NM_052814.3:c.184+38A=	NP_434701.1:n.184+38A=
NM_052813.5:c.184+38A= MANE Select	NP_434700.2:n.184+38A=
NM_052814.4:c.184+38A=	NP_434701.1:n.184+38A=