Canonical Allele Identifier: CA3173162470
Community Standard Title: NM_052813.5(CARD9):c.424G= (p.Asp142=)
Gene: CARD9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136371044C= , CM000671.2:g.136371044C= GRCh38
NC_000009.11:g.139265496C= , CM000671.1:g.139265496C= GRCh37
NC_000009.10:g.138385317C= NCBI36
NG_021197.1:g.7638G= , LRG_178:g.7638G=

Transcript Alleles

HGVS Amino-acid Change
NM_052813.5:c.424G= MANE Select NP_434700.2:p.Asp142=
ENST00000371732.10:c.424G= MANE Select ENSP00000360797.5:p.Asp142=
NM_052813.4:c.424G= , LRG_178t1:c.424G= NP_434700.2:p.Asp142=
NM_052814.3:c.424G= NP_434701.1:p.Asp142=
NM_052814.4:c.424G= NP_434701.1:p.Asp142=
ENST00000371732.9:c.424G= ENSP00000360797.5:p.Asp142=
ENST00000371734.7:c.424G= ENSP00000360799.3:p.Asp142=
ENST00000481053.5:n.553G=
ENST00000489932.2:c.424G= ENSP00000451368.1:p.Asp142=
ENST00000556340.1:n.555G=
ENST00000641290.1:c.112G= ENSP00000493113.1:p.Asp38=
ENST00000641290.2:n.429G=
ENST00000695905.1:n.552G=
ENST00000695906.1:n.552G=
ENST00000695908.1:n.543G=
ENST00000696169.1:c.424G= ENSP00000512460.1:p.Asp142=