Canonical Allele Identifier: CA2753941558
Gene: CTLA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203871553_203871554insCACACCCAACAC , CM000664.2:g.203871553_203871554insCACACCCAACAC GRCh38
NC_000002.11:g.204736276_204736277insCACACCCAACAC , CM000664.1:g.204736276_204736277insCACACCCAACAC GRCh37
NC_000002.10:g.204444521_204444522insCACACCCAACAC NCBI36
NG_011502.1:g.8768_8769insCACACCCAACAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000696049.1:c.507+126_507+127insCACACCCAACAC ENSP00000512353.1:n.507+126_507+127insCACACCCAACAC
ENST00000696479.1:c.639+66_639+67insCACACCCAACAC ENSP00000512655.1:n.639+66_639+67insCACACCCAACAC
ENST00000427473.3:n.491+620_491+621insCACACCCAACAC
ENST00000648405.2:c.567+66_567+67insCACACCCAACAC MANE Select ENSP00000497102.1:n.567+66_567+67insCACACCCAACAC
ENST00000650075.1:n.591+66_591+67insCACACCCAACAC
ENST00000295854.10:c.457+620_457+621insCACACCCAACAC ENSP00000295854.6:n.457+620_457+621insCACACCCAACAC
ENST00000302823.7:c.567+66_567+67insCACACCCAACAC ENSP00000303939.3:n.567+66_567+67insCACACCCAACAC
ENST00000427473.2:c.346+620_346+621insCACACCCAACAC ENSP00000409707.2:n.346+620_346+621insCACACCCAACAC
ENST00000472206.1:c.172+905_172+906insCACACCCAACAC ENSP00000417779.1:n.172+905_172+906insCACACCCAACAC
ENST00000487393.1:n.110-1155_110-1154insCACACCCAACAC
NM_001037631.2:c.457+620_457+621insCACACCCAACAC NP_001032720.1:n.457+620_457+621insCACACCCAACAC
NM_005214.4:c.567+66_567+67insCACACCCAACAC NP_005205.2:n.567+66_567+67insCACACCCAACAC
XR_241294.1:n.707+66_707+67insCACACCCAACAC
NM_001037631.3:c.457+620_457+621insCACACCCAACAC NP_001032720.1:n.457+620_457+621insCACACCCAACAC
NM_005214.5:c.567+66_567+67insCACACCCAACAC MANE Select NP_005205.2:n.567+66_567+67insCACACCCAACAC