Canonical Allele Identifier: CA2580613256

Gene: CARD14

Linked Data

• ClinVar Variation Id: 2044564
• ClinVar RCV Id: RCV002903782
• gnomAD v4: 17-80184230-C-CAGG

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80184237_80184239dup , CM000679.2:g.80184237_80184239dup	GRCh38
NC_000017.10:g.78158036_78158038dup , CM000679.1:g.78158036_78158038dup	GRCh37
NC_000017.9:g.75772631_75772633dup	NCBI36
NG_032778.1:g.19246_19248dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000571427.2:c.674_675+1dup
ENST00000703566.1:c.674_675+1dup
ENST00000703567.1:c.674_675+1dup
ENST00000703568.1:c.674_675+1dup
ENST00000703569.1:n.875_876+1dup
ENST00000648128.1:c.246_247+1dup
ENST00000648509.2:c.674_675+1dup
ENST00000650806.1:n.916_917+1dup
ENST00000650867.1:c.674_675+1dup
ENST00000651068.1:c.674_675+1dup
ENST00000651388.1:c.674_675+1dup
ENST00000651672.1:c.674_675+1dup
ENST00000652599.1:n.1110_1111+1dup
ENST00000344227.6:c.674_675+1dup
ENST00000570421.5:c.674_675+1dup
ENST00000571450.1:c.63_64+1dup
ENST00000572838.1:n.87_88+1dup
ENST00000573882.5:c.674_675+1dup
ENST00000575500.5:c.674_675+1dup
NM_001257970.1:c.674_675+1dup
NM_024110.4:c.674_675+1dup
NR_047566.1:n.907_908+1dup
XM_011525212.1:c.674_675+1dup
XM_011525213.1:c.674_675+1dup
XM_011525214.1:c.674_675+1dup
XM_011525215.1:c.674_675+1dup
XM_011525216.1:c.674_675+1dup
XM_011525217.1:c.674_675+1dup
XM_011525218.1:c.674_675+1dup
XM_011525219.1:c.674_675+1dup
XM_011525220.1:c.674_675+1dup
XM_011525221.1:c.674_675+1dup
XM_011525222.1:c.674_675+1dup
XM_011525223.1:c.674_675+1dup
XR_934547.1:n.814_815+1dup
NM_001366385.1:c.674_675+1dup
XM_011525218.2:c.674_675+1dup
XM_024450934.1:c.674_675+1dup
XM_024450935.1:c.674_675+1dup
XM_024450936.1:c.674_675+1dup
XM_024450937.1:c.674_675+1dup
XR_002958065.1:n.814_815+1dup
XR_002958066.1:n.814_815+1dup
NR_047566.2:n.869_870+1dup