Canonical Allele Identifier: CA2662768840

Gene: CTLA4

Linked Data

• gnomAD v4: 2-203871499-G-GCACCATCAGCACCACA

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203871500_203871501insACCATCAGCACCACAC , CM000664.2:g.203871500_203871501insACCATCAGCACCACAC	GRCh38
NC_000002.11:g.204736223_204736224insACCATCAGCACCACAC , CM000664.1:g.204736223_204736224insACCATCAGCACCACAC	GRCh37
NC_000002.10:g.204444468_204444469insACCATCAGCACCACAC	NCBI36
NG_011502.1:g.8715_8716insACCATCAGCACCACAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696049.1:c.507+73_507+74insACCATCAGCACCACAC	ENSP00000512353.1:n.507+73_507+74insACCATCAGCACCACAC
ENST00000696479.1:c.639+13_639+14insACCATCAGCACCACAC	ENSP00000512655.1:n.639+13_639+14insACCATCAGCACCACAC
ENST00000427473.3:n.491+567_491+568insACCATCAGCACCACAC
ENST00000648405.2:c.567+13_567+14insACCATCAGCACCACAC MANE Select	ENSP00000497102.1:n.567+13_567+14insACCATCAGCACCACAC
ENST00000650075.1:n.591+13_591+14insACCATCAGCACCACAC
ENST00000295854.10:c.457+567_457+568insACCATCAGCACCACAC	ENSP00000295854.6:n.457+567_457+568insACCATCAGCACCACAC
ENST00000302823.7:c.567+13_567+14insACCATCAGCACCACAC	ENSP00000303939.3:n.567+13_567+14insACCATCAGCACCACAC
ENST00000427473.2:c.346+567_346+568insACCATCAGCACCACAC	ENSP00000409707.2:n.346+567_346+568insACCATCAGCACCACAC
ENST00000472206.1:c.172+852_172+853insACCATCAGCACCACAC	ENSP00000417779.1:n.172+852_172+853insACCATCAGCACCACAC
ENST00000487393.1:n.110-1208_110-1207insACCATCAGCACCACAC
NM_001037631.2:c.457+567_457+568insACCATCAGCACCACAC	NP_001032720.1:n.457+567_457+568insACCATCAGCACCACAC
NM_005214.4:c.567+13_567+14insACCATCAGCACCACAC	NP_005205.2:n.567+13_567+14insACCATCAGCACCACAC
XR_241294.1:n.707+13_707+14insACCATCAGCACCACAC
NM_001037631.3:c.457+567_457+568insACCATCAGCACCACAC	NP_001032720.1:n.457+567_457+568insACCATCAGCACCACAC
NM_005214.5:c.567+13_567+14insACCATCAGCACCACAC MANE Select	NP_005205.2:n.567+13_567+14insACCATCAGCACCACAC