Canonical Allele Identifier: CA2573320283
Gene: CTLA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203871491del , CM000664.2:g.203871491del GRCh38
NC_000002.11:g.204736214del , CM000664.1:g.204736214del GRCh37
NC_000002.10:g.204444459del NCBI36
NG_011502.1:g.8706del

Transcript Alleles

HGVS Amino-acid Change
ENST00000696049.1:c.507+64del ENSP00000512353.1:n.507+64del
ENST00000696479.1:c.639+4del ENSP00000512655.1:n.639+4del
ENST00000427473.3:n.491+558del
ENST00000648405.2:c.567+4del MANE Select ENSP00000497102.1:n.567+4del
ENST00000650075.1:n.591+4del
ENST00000295854.10:c.457+558del ENSP00000295854.6:n.457+558del
ENST00000302823.7:c.567+4del ENSP00000303939.3:n.567+4del
ENST00000427473.2:c.346+558del ENSP00000409707.2:n.346+558del
ENST00000472206.1:c.172+843del ENSP00000417779.1:n.172+843del
ENST00000487393.1:n.110-1217del
NM_001037631.2:c.457+558del NP_001032720.1:n.457+558del
NM_005214.4:c.567+4del NP_005205.2:n.567+4del
XR_241294.1:n.707+4del
NM_001037631.3:c.457+558del NP_001032720.1:n.457+558del
NM_005214.5:c.567+4del MANE Select NP_005205.2:n.567+4del