Canonical Allele Identifier: CA10603326
Gene: CARD14 HGNC NCBI

Linked Data

ClinVar Variation Id: 280130
ClinVar RCV Id: RCV000029231 RCV000262256 RCV001855059
dbSNP Id: rs886041402
COSMIC: COSM5741172
MyVariant Identifiers: chr17:g.78156590G>A (hg19) chr17:g.80182791G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.80182791G>A , CM000679.2:g.80182791G>A GRCh38
NC_000017.10:g.78156590G>A , CM000679.1:g.78156590G>A GRCh37
NC_000017.9:g.75771185G>A NCBI36
NG_032778.1:g.17800G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000571427.2:c.349+1G>A ENSP00000516501.1:n.349+1G>A
ENST00000703566.1:c.349+1G>A ENSP00000515382.1:n.349+1G>A
ENST00000703567.1:c.349+1G>A ENSP00000515383.1:n.349+1G>A
ENST00000703568.1:c.349+1G>A ENSP00000515384.1:n.349+1G>A
ENST00000703569.1:n.550+1G>A
ENST00000648509.2:c.349+1G>A MANE Select ENSP00000498071.1:n.349+1G>A
ENST00000650806.1:n.591+1G>A
ENST00000650867.1:c.349+1G>A ENSP00000498570.1:n.349+1G>A
ENST00000651068.1:c.349+1G>A ENSP00000498274.1:n.349+1G>A
ENST00000651388.1:c.349+1G>A ENSP00000498956.1:n.349+1G>A
ENST00000651672.1:c.349+1G>A ENSP00000499145.1:n.349+1G>A
ENST00000652599.1:n.785+1G>A
ENST00000344227.6:c.349+1G>A ENSP00000344549.2:n.349+1G>A
ENST00000570421.5:c.349+1G>A ENSP00000461806.1:n.349+1G>A
ENST00000573882.5:c.349+1G>A ENSP00000458715.1:n.349+1G>A
ENST00000575500.5:c.349+1G>A ENSP00000460883.1:n.349+1G>A
NM_001257970.1:c.349+1G>A NP_001244899.1:n.349+1G>A
NM_024110.4:c.349+1G>A NP_077015.2:n.349+1G>A
NR_047566.1:n.582+1G>A
XM_011525212.1:c.349+1G>A XP_011523514.1:n.349+1G>A
XM_011525213.1:c.349+1G>A XP_011523515.1:n.349+1G>A
XM_011525214.1:c.349+1G>A XP_011523516.1:n.349+1G>A
XM_011525215.1:c.349+1G>A XP_011523517.1:n.349+1G>A
XM_011525216.1:c.349+1G>A XP_011523518.1:n.349+1G>A
XM_011525217.1:c.349+1G>A XP_011523519.1:n.349+1G>A
XM_011525218.1:c.349+1G>A XP_011523520.1:n.349+1G>A
XM_011525219.1:c.349+1G>A XP_011523521.1:n.349+1G>A
XM_011525220.1:c.349+1G>A XP_011523522.1:n.349+1G>A
XM_011525221.1:c.349+1G>A XP_011523523.1:n.349+1G>A
XM_011525222.1:c.349+1G>A XP_011523524.1:n.349+1G>A
XM_011525223.1:c.349+1G>A XP_011523525.1:n.349+1G>A
XR_934547.1:n.489+1G>A
NM_001366385.1:c.349+1G>A MANE Select NP_001353314.1:n.349+1G>A
XM_011525218.2:c.349+1G>A XP_011523520.1:n.349+1G>A
XM_024450934.1:c.349+1G>A XP_024306702.1:n.349+1G>A
XM_024450935.1:c.349+1G>A XP_024306703.1:n.349+1G>A
XM_024450936.1:c.349+1G>A XP_024306704.1:n.349+1G>A
XM_024450937.1:c.349+1G>A XP_024306705.1:n.349+1G>A
XR_002958065.1:n.489+1G>A
XR_002958066.1:n.489+1G>A
NR_047566.2:n.544+1G>A
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