Canonical Allele Identifier: CA2277849577

Gene: CARD14

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80183776_80183784delinsCCGCCCACA , CM000679.2:g.80183776_80183784delinsCCGCCCACA	GRCh38
NC_000017.10:g.78157575_78157583delinsCCGCCCACA , CM000679.1:g.78157575_78157583delinsCCGCCCACA	GRCh37
NC_000017.9:g.75772170_75772178delinsCCGCCCACA	NCBI36
NG_032778.1:g.18785_18793delinsCCGCCCACA

Transcript Alleles

HGVS	Amino-acid change
ENST00000571427.2:c.350-137_350-129delinsCCGCCCACA	ENSP00000516501.1:n.350-137_350-129delinsCCGCCCACA
ENST00000703566.1:c.350-137_350-129delinsCCGCCCACA	ENSP00000515382.1:n.350-137_350-129delinsCCGCCCACA
ENST00000703567.1:c.350-137_350-129delinsCCGCCCACA	ENSP00000515383.1:n.350-137_350-129delinsCCGCCCACA
ENST00000703568.1:c.350-137_350-129delinsCCGCCCACA	ENSP00000515384.1:n.350-137_350-129delinsCCGCCCACA
ENST00000703569.1:n.551-137_551-129delinsCCGCCCACA
ENST00000648509.2:c.350-137_350-129delinsCCGCCCACA MANE Select	ENSP00000498071.1:n.350-137_350-129delinsCCGCCCACA
ENST00000650806.1:n.592-137_592-129delinsCCGCCCACA
ENST00000650867.1:c.350-137_350-129delinsCCGCCCACA	ENSP00000498570.1:n.350-137_350-129delinsCCGCCCACA
ENST00000651068.1:c.350-137_350-129delinsCCGCCCACA	ENSP00000498274.1:n.350-137_350-129delinsCCGCCCACA
ENST00000651388.1:c.350-137_350-129delinsCCGCCCACA	ENSP00000498956.1:n.350-137_350-129delinsCCGCCCACA
ENST00000651672.1:c.350-137_350-129delinsCCGCCCACA	ENSP00000499145.1:n.350-137_350-129delinsCCGCCCACA
ENST00000652599.1:n.786-137_786-129delinsCCGCCCACA
ENST00000344227.6:c.350-137_350-129delinsCCGCCCACA	ENSP00000344549.2:n.350-137_350-129delinsCCGCCCACA
ENST00000570421.5:c.350-137_350-129delinsCCGCCCACA	ENSP00000461806.1:n.350-137_350-129delinsCCGCCCACA
ENST00000573882.5:c.350-137_350-129delinsCCGCCCACA	ENSP00000458715.1:n.350-137_350-129delinsCCGCCCACA
ENST00000575500.5:c.350-137_350-129delinsCCGCCCACA	ENSP00000460883.1:n.350-137_350-129delinsCCGCCCACA
NM_001257970.1:c.350-137_350-129delinsCCGCCCACA	NP_001244899.1:n.350-137_350-129delinsCCGCCCACA
NM_024110.4:c.350-137_350-129delinsCCGCCCACA	NP_077015.2:n.350-137_350-129delinsCCGCCCACA
NR_047566.1:n.583-137_583-129delinsCCGCCCACA
XM_011525212.1:c.350-137_350-129delinsCCGCCCACA	XP_011523514.1:n.350-137_350-129delinsCCGCCCACA
XM_011525213.1:c.350-137_350-129delinsCCGCCCACA	XP_011523515.1:n.350-137_350-129delinsCCGCCCACA
XM_011525214.1:c.350-137_350-129delinsCCGCCCACA	XP_011523516.1:n.350-137_350-129delinsCCGCCCACA
XM_011525215.1:c.350-137_350-129delinsCCGCCCACA	XP_011523517.1:n.350-137_350-129delinsCCGCCCACA
XM_011525216.1:c.350-137_350-129delinsCCGCCCACA	XP_011523518.1:n.350-137_350-129delinsCCGCCCACA
XM_011525217.1:c.350-137_350-129delinsCCGCCCACA	XP_011523519.1:n.350-137_350-129delinsCCGCCCACA
XM_011525218.1:c.350-137_350-129delinsCCGCCCACA	XP_011523520.1:n.350-137_350-129delinsCCGCCCACA
XM_011525219.1:c.350-137_350-129delinsCCGCCCACA	XP_011523521.1:n.350-137_350-129delinsCCGCCCACA
XM_011525220.1:c.350-137_350-129delinsCCGCCCACA	XP_011523522.1:n.350-137_350-129delinsCCGCCCACA
XM_011525221.1:c.350-137_350-129delinsCCGCCCACA	XP_011523523.1:n.350-137_350-129delinsCCGCCCACA
XM_011525222.1:c.350-137_350-129delinsCCGCCCACA	XP_011523524.1:n.350-137_350-129delinsCCGCCCACA
XM_011525223.1:c.350-137_350-129delinsCCGCCCACA	XP_011523525.1:n.350-137_350-129delinsCCGCCCACA
XR_934547.1:n.490-137_490-129delinsCCGCCCACA
NM_001366385.1:c.350-137_350-129delinsCCGCCCACA MANE Select	NP_001353314.1:n.350-137_350-129delinsCCGCCCACA
XM_011525218.2:c.350-137_350-129delinsCCGCCCACA	XP_011523520.1:n.350-137_350-129delinsCCGCCCACA
XM_024450934.1:c.350-137_350-129delinsCCGCCCACA	XP_024306702.1:n.350-137_350-129delinsCCGCCCACA
XM_024450935.1:c.350-137_350-129delinsCCGCCCACA	XP_024306703.1:n.350-137_350-129delinsCCGCCCACA
XM_024450936.1:c.350-137_350-129delinsCCGCCCACA	XP_024306704.1:n.350-137_350-129delinsCCGCCCACA
XM_024450937.1:c.350-137_350-129delinsCCGCCCACA	XP_024306705.1:n.350-137_350-129delinsCCGCCCACA
XR_002958065.1:n.490-137_490-129delinsCCGCCCACA
XR_002958066.1:n.490-137_490-129delinsCCGCCCACA
NR_047566.2:n.545-137_545-129delinsCCGCCCACA