Canonical Allele Identifier: CA2662768770
Gene: CTLA4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203871247del , CM000664.2:g.203871247del GRCh38
NC_000002.11:g.204735970del , CM000664.1:g.204735970del GRCh37
NC_000002.10:g.204444215del NCBI36
NG_011502.1:g.8462del

Transcript Alleles

HGVS Amino-acid Change
ENST00000696049.1:c.458-131del ENSP00000512353.1:n.458-131del
ENST00000696479.1:c.530-131del ENSP00000512655.1:n.530-131del
ENST00000427473.3:n.491+314del
ENST00000648405.2:c.458-131del MANE Select ENSP00000497102.1:n.458-131del
ENST00000650075.1:n.482-131del
ENST00000295854.10:c.457+314del ENSP00000295854.6:n.457+314del
ENST00000302823.7:c.458-131del ENSP00000303939.3:n.458-131del
ENST00000427473.2:c.346+314del ENSP00000409707.2:n.346+314del
ENST00000472206.1:c.172+599del ENSP00000417779.1:n.172+599del
ENST00000487393.1:n.110-1461del
NM_001037631.2:c.457+314del NP_001032720.1:n.457+314del
NM_005214.4:c.458-131del NP_005205.2:n.458-131del
XR_241294.1:n.598-131del
NM_001037631.3:c.457+314del NP_001032720.1:n.457+314del
NM_005214.5:c.458-131del MANE Select NP_005205.2:n.458-131del