Canonical Allele Identifier: CA2662768839

Gene: CTLA4

Linked Data

• gnomAD v4: 2-203871494-GTGGTGCTGA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203871501_203871509del , CM000664.2:g.203871501_203871509del	GRCh38
NC_000002.11:g.204736224_204736232del , CM000664.1:g.204736224_204736232del	GRCh37
NC_000002.10:g.204444469_204444477del	NCBI36
NG_011502.1:g.8716_8724del

Transcript Alleles

HGVS	Amino-acid change
ENST00000696049.1:c.507+74_507+82del	ENSP00000512353.1:n.507+74_507+82del
ENST00000696479.1:c.639+14_639+22del	ENSP00000512655.1:n.639+14_639+22del
ENST00000427473.3:n.491+568_491+576del
ENST00000648405.2:c.567+14_567+22del MANE Select	ENSP00000497102.1:n.567+14_567+22del
ENST00000650075.1:n.591+14_591+22del
ENST00000295854.10:c.457+568_457+576del	ENSP00000295854.6:n.457+568_457+576del
ENST00000302823.7:c.567+14_567+22del	ENSP00000303939.3:n.567+14_567+22del
ENST00000427473.2:c.346+568_346+576del	ENSP00000409707.2:n.346+568_346+576del
ENST00000472206.1:c.172+853_172+861del	ENSP00000417779.1:n.172+853_172+861del
ENST00000487393.1:n.110-1207_110-1199del
NM_001037631.2:c.457+568_457+576del	NP_001032720.1:n.457+568_457+576del
NM_005214.4:c.567+14_567+22del	NP_005205.2:n.567+14_567+22del
XR_241294.1:n.707+14_707+22del
NM_001037631.3:c.457+568_457+576del	NP_001032720.1:n.457+568_457+576del
NM_005214.5:c.567+14_567+22del MANE Select	NP_005205.2:n.567+14_567+22del