Canonical Allele Identifier: CA129844
Gene: CARD14 HGNC NCBI

Linked Data

ClinVar Variation Id: 31609
dbSNP Id: rs281875214

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.80183976A>C , CM000679.2:g.80183976A>C GRCh38
NC_000017.10:g.78157775A>C , CM000679.1:g.78157775A>C GRCh37
NC_000017.9:g.75772370A>C NCBI36
NG_032778.1:g.18985A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000648509.2:c.413A>C MANE Select ENSP00000498071.1:p.Glu138Ala
ENST00000650806.1:n.655A>C
ENST00000650867.1:c.413A>C ENSP00000498570.1:p.Glu138Ala
ENST00000651068.1:c.413A>C ENSP00000498274.1:p.Glu138Ala
ENST00000651388.1:c.413A>C ENSP00000498956.1:p.Glu138Ala
ENST00000651672.1:c.413A>C ENSP00000499145.1:p.Glu138Ala
ENST00000652599.1:n.849A>C
ENST00000344227.6:c.413A>C ENSP00000344549.2:p.Glu138Ala
ENST00000570421.5:c.413A>C ENSP00000461806.1:p.Glu138Ala
ENST00000573882.5:c.413A>C ENSP00000458715.1:p.Glu138Ala
ENST00000575500.5:c.413A>C ENSP00000460883.1:p.Glu138Ala
NM_001257970.1:c.413A>C NP_001244899.1:p.Glu138Ala
NM_024110.4:c.413A>C NP_077015.2:p.Glu138Ala
NR_047566.1:n.646A>C
XM_011525212.1:c.413A>C XP_011523514.1:p.Glu138Ala
XM_011525213.1:c.413A>C XP_011523515.1:p.Glu138Ala
XM_011525214.1:c.413A>C XP_011523516.1:p.Glu138Ala
XM_011525215.1:c.413A>C XP_011523517.1:p.Glu138Ala
XM_011525216.1:c.413A>C XP_011523518.1:p.Glu138Ala
XM_011525217.1:c.413A>C XP_011523519.1:p.Glu138Ala
XM_011525218.1:c.413A>C XP_011523520.1:p.Glu138Ala
XM_011525219.1:c.413A>C XP_011523521.1:p.Glu138Ala
XM_011525220.1:c.413A>C XP_011523522.1:p.Glu138Ala
XM_011525221.1:c.413A>C XP_011523523.1:p.Glu138Ala
XM_011525222.1:c.413A>C XP_011523524.1:p.Glu138Ala
XM_011525223.1:c.413A>C XP_011523525.1:p.Glu138Ala
XR_934547.1:n.553A>C
NM_001366385.1:c.413A>C MANE Select NP_001353314.1:p.Glu138Ala
XM_011525218.2:c.413A>C XP_011523520.1:p.Glu138Ala
XM_024450934.1:c.413A>C XP_024306702.1:p.Glu138Ala
XM_024450935.1:c.413A>C XP_024306703.1:p.Glu138Ala
XM_024450936.1:c.413A>C XP_024306704.1:p.Glu138Ala
XM_024450937.1:c.413A>C XP_024306705.1:p.Glu138Ala
XR_002958065.1:n.553A>C
XR_002958066.1:n.553A>C
NR_047566.2:n.608A>C