Canonical Allele Identifier: CA1130007747

Gene: CARD9

Linked Data

• dbSNP Id: rs1833286834
• gnomAD v4: 9-136371952-CG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136371956del , CM000671.2:g.136371956del	GRCh38
NC_000009.11:g.139266408del , CM000671.1:g.139266408del	GRCh37
NC_000009.10:g.138386229del	NCBI36
NG_021197.1:g.6729del , LRG_178:g.6729del

Transcript Alleles

HGVS	Amino-acid change
ENST00000641290.2:n.131del
ENST00000695905.1:n.254del
ENST00000695906.1:n.254del
ENST00000695908.1:n.245del
ENST00000696169.1:c.126del	ENSP00000512460.1:p.Asp43MetfsTer?
ENST00000371732.10:c.126del MANE Select	ENSP00000360797.5:p.Asp43MetfsTer?
ENST00000641290.1:c.-187del	ENSP00000493113.1:n.-187del
ENST00000371732.9:c.126del	ENSP00000360797.5:p.Asp43MetfsTer?
ENST00000371734.7:c.126del	ENSP00000360799.3:p.Asp43MetfsTer?
ENST00000481053.5:n.255del
ENST00000489932.2:c.126del	ENSP00000451368.1:p.Asp43MetfsTer?
ENST00000556340.1:n.257del
NM_052813.4:c.126del , LRG_178t1:c.126del	NP_434700.2:p.Asp43MetfsTer?
NM_052814.3:c.126del	NP_434701.1:p.Asp43MetfsTer?
NM_052813.5:c.126del MANE Select	NP_434700.2:p.Asp43MetfsTer?
NM_052814.4:c.126del	NP_434701.1:p.Asp43MetfsTer?