Canonical Allele Identifier: CA2640297615

Gene: CARD14

Linked Data

• gnomAD v4: 17-80184247-A-ACACCCTG

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80184253_80184259dup , CM000679.2:g.80184253_80184259dup	GRCh38
NC_000017.10:g.78158052_78158058dup , CM000679.1:g.78158052_78158058dup	GRCh37
NC_000017.9:g.75772647_75772653dup	NCBI36
NG_032778.1:g.19262_19268dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000571427.2:c.675+15_675+21dup	ENSP00000516501.1:n.675+15_675+21dup
ENST00000703566.1:c.675+15_675+21dup	ENSP00000515382.1:n.675+15_675+21dup
ENST00000703567.1:c.675+15_675+21dup	ENSP00000515383.1:n.675+15_675+21dup
ENST00000703568.1:c.675+15_675+21dup	ENSP00000515384.1:n.675+15_675+21dup
ENST00000703569.1:n.876+15_876+21dup
ENST00000648128.1:c.247+15_247+21dup
ENST00000648509.2:c.675+15_675+21dup MANE Select	ENSP00000498071.1:n.675+15_675+21dup
ENST00000650806.1:n.917+15_917+21dup
ENST00000650867.1:c.675+15_675+21dup	ENSP00000498570.1:n.675+15_675+21dup
ENST00000651068.1:c.675+15_675+21dup	ENSP00000498274.1:n.675+15_675+21dup
ENST00000651388.1:c.675+15_675+21dup	ENSP00000498956.1:n.675+15_675+21dup
ENST00000651672.1:c.675+15_675+21dup	ENSP00000499145.1:n.675+15_675+21dup
ENST00000652599.1:n.1111+15_1111+21dup
ENST00000344227.6:c.675+15_675+21dup	ENSP00000344549.2:n.675+15_675+21dup
ENST00000570421.5:c.675+15_675+21dup	ENSP00000461806.1:n.675+15_675+21dup
ENST00000571450.1:c.64+15_64+21dup
ENST00000572838.1:n.88+15_88+21dup
ENST00000573882.5:c.675+15_675+21dup	ENSP00000458715.1:n.675+15_675+21dup
ENST00000575500.5:c.675+15_675+21dup	ENSP00000460883.1:n.675+15_675+21dup
NM_001257970.1:c.675+15_675+21dup	NP_001244899.1:n.675+15_675+21dup
NM_024110.4:c.675+15_675+21dup	NP_077015.2:n.675+15_675+21dup
NR_047566.1:n.908+15_908+21dup
XM_011525212.1:c.675+15_675+21dup	XP_011523514.1:n.675+15_675+21dup
XM_011525213.1:c.675+15_675+21dup	XP_011523515.1:n.675+15_675+21dup
XM_011525214.1:c.675+15_675+21dup	XP_011523516.1:n.675+15_675+21dup
XM_011525215.1:c.675+15_675+21dup	XP_011523517.1:n.675+15_675+21dup
XM_011525216.1:c.675+15_675+21dup	XP_011523518.1:n.675+15_675+21dup
XM_011525217.1:c.675+15_675+21dup	XP_011523519.1:n.675+15_675+21dup
XM_011525218.1:c.675+15_675+21dup	XP_011523520.1:n.675+15_675+21dup
XM_011525219.1:c.675+15_675+21dup	XP_011523521.1:n.675+15_675+21dup
XM_011525220.1:c.675+15_675+21dup	XP_011523522.1:n.675+15_675+21dup
XM_011525221.1:c.675+15_675+21dup	XP_011523523.1:n.675+15_675+21dup
XM_011525222.1:c.675+15_675+21dup	XP_011523524.1:n.675+15_675+21dup
XM_011525223.1:c.675+15_675+21dup	XP_011523525.1:n.675+15_675+21dup
XR_934547.1:n.815+15_815+21dup
NM_001366385.1:c.675+15_675+21dup MANE Select	NP_001353314.1:n.675+15_675+21dup
XM_011525218.2:c.675+15_675+21dup	XP_011523520.1:n.675+15_675+21dup
XM_024450934.1:c.675+15_675+21dup	XP_024306702.1:n.675+15_675+21dup
XM_024450935.1:c.675+15_675+21dup	XP_024306703.1:n.675+15_675+21dup
XM_024450936.1:c.675+15_675+21dup	XP_024306704.1:n.675+15_675+21dup
XM_024450937.1:c.675+15_675+21dup	XP_024306705.1:n.675+15_675+21dup
XR_002958065.1:n.815+15_815+21dup
XR_002958066.1:n.815+15_815+21dup
NR_047566.2:n.870+15_870+21dup