Canonical Allele Identifier: CA2662768894

Gene: CTLA4

Linked Data

• gnomAD v4: 2-203871577-T-TTGAGA

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203871587_203871591dup , CM000664.2:g.203871587_203871591dup	GRCh38
NC_000002.11:g.204736310_204736314dup , CM000664.1:g.204736310_204736314dup	GRCh37
NC_000002.10:g.204444555_204444559dup	NCBI36
NG_011502.1:g.8802_8806dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696049.1:c.507+160_507+164dup	ENSP00000512353.1:n.507+160_507+164dup
ENST00000696479.1:c.639+100_639+104dup	ENSP00000512655.1:n.639+100_639+104dup
ENST00000427473.3:n.491+654_491+658dup
ENST00000648405.2:c.567+100_567+104dup MANE Select	ENSP00000497102.1:n.567+100_567+104dup
ENST00000650075.1:n.591+100_591+104dup
ENST00000295854.10:c.457+654_457+658dup	ENSP00000295854.6:n.457+654_457+658dup
ENST00000302823.7:c.567+100_567+104dup	ENSP00000303939.3:n.567+100_567+104dup
ENST00000427473.2:c.346+654_346+658dup	ENSP00000409707.2:n.346+654_346+658dup
ENST00000472206.1:c.172+939_172+943dup	ENSP00000417779.1:n.172+939_172+943dup
ENST00000487393.1:n.110-1121_110-1117dup
NM_001037631.2:c.457+654_457+658dup	NP_001032720.1:n.457+654_457+658dup
NM_005214.4:c.567+100_567+104dup	NP_005205.2:n.567+100_567+104dup
XR_241294.1:n.707+100_707+104dup
NM_001037631.3:c.457+654_457+658dup	NP_001032720.1:n.457+654_457+658dup
NM_005214.5:c.567+100_567+104dup MANE Select	NP_005205.2:n.567+100_567+104dup