Canonical Allele Identifier: CA1884181495

Gene: CARD9

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136367788C= , CM000671.2:g.136367788C=	GRCh38
NC_000009.11:g.139262240C= , CM000671.1:g.139262240C=	GRCh37
NC_000009.10:g.138382061C=	NCBI36
NG_021197.1:g.10894G= , LRG_178:g.10894G=

Transcript Alleles

HGVS	Amino-acid Change
NM_052813.5:c.1118G= MANE Select	NP_434700.2:p.Arg373=
ENST00000371732.10:c.1118G= MANE Select	ENSP00000360797.5:p.Arg373=
NM_052813.4:c.1118G= , LRG_178t1:c.1118G=	NP_434700.2:p.Arg373=
NM_052814.3:c.1118G=	NP_434701.1:p.Arg373=
NM_052814.4:c.1118G=	NP_434701.1:p.Arg373=
ENST00000371732.9:c.1118G=	ENSP00000360797.5:p.Arg373=
ENST00000371734.7:c.1118G=	ENSP00000360799.3:p.Arg373=
ENST00000481053.5:n.1395G=
ENST00000485975.1:n.1194G=
ENST00000489932.2:c.*165G=	ENSP00000451368.1:n.*165G=
ENST00000641290.2:n.1123G=
ENST00000695905.1:n.1246G=
ENST00000695906.1:n.1246G=
ENST00000695907.1:n.17G=
ENST00000696169.1:c.*165G=	ENSP00000512460.1:n.*165G=