Canonical Allele Identifier: CA2662768842

Gene: CTLA4

Linked Data

• gnomAD v4: 2-203871500-C-CACCA

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203871500_203871501insACCA , CM000664.2:g.203871500_203871501insACCA	GRCh38
NC_000002.11:g.204736223_204736224insACCA , CM000664.1:g.204736223_204736224insACCA	GRCh37
NC_000002.10:g.204444468_204444469insACCA	NCBI36
NG_011502.1:g.8715_8716insACCA

Transcript Alleles

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