Canonical Allele Identifier: CA2577220136
Gene: CTLA4 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203871517_203871519del , CM000664.2:g.203871517_203871519del GRCh38
NC_000002.11:g.204736240_204736242del , CM000664.1:g.204736240_204736242del GRCh37
NC_000002.10:g.204444485_204444487del NCBI36
NG_011502.1:g.8732_8734del

Transcript Alleles

HGVS Amino-acid change
ENST00000696049.1:c.507+90_507+92del ENSP00000512353.1:n.507+90_507+92del
ENST00000696479.1:c.639+30_639+32del ENSP00000512655.1:n.639+30_639+32del
ENST00000427473.3:n.491+584_491+586del
ENST00000648405.2:c.567+30_567+32del MANE Select ENSP00000497102.1:n.567+30_567+32del
ENST00000650075.1:n.591+30_591+32del
ENST00000295854.10:c.457+584_457+586del ENSP00000295854.6:n.457+584_457+586del
ENST00000302823.7:c.567+30_567+32del ENSP00000303939.3:n.567+30_567+32del
ENST00000427473.2:c.346+584_346+586del ENSP00000409707.2:n.346+584_346+586del
ENST00000472206.1:c.172+869_172+871del ENSP00000417779.1:n.172+869_172+871del
ENST00000487393.1:n.110-1191_110-1189del
NM_001037631.2:c.457+584_457+586del NP_001032720.1:n.457+584_457+586del
NM_005214.4:c.567+30_567+32del NP_005205.2:n.567+30_567+32del
XR_241294.1:n.707+30_707+32del
NM_001037631.3:c.457+584_457+586del NP_001032720.1:n.457+584_457+586del
NM_005214.5:c.567+30_567+32del MANE Select NP_005205.2:n.567+30_567+32del
Search 100 bp 5'
Search 100 bp 3'