Canonical Allele Identifier: CA1322148571
Gene: CTLA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203867936_203867937delinsTA , CM000664.2:g.203867936_203867937delinsTA GRCh38
NC_000002.11:g.204732659_204732660delinsTA , CM000664.1:g.204732659_204732660delinsTA GRCh37
NC_000002.10:g.204440904_204440905delinsTA NCBI36
NG_011502.1:g.5151_5152delinsTA

Transcript Alleles

HGVS Amino-acid change
ENST00000696049.1:c.-7_-6delinsTA ENSP00000512353.1:n.-7_-6delinsTA
ENST00000696479.1:c.66_67delinsTA ENSP00000512655.1:p.His22=
ENST00000648405.2:c.-7_-6delinsTA MANE Select ENSP00000497102.1:n.-7_-6delinsTA
ENST00000302823.7:c.-7_-6delinsTA ENSP00000303939.3:n.-7_-6delinsTA
NM_001037631.2:c.-7_-6delinsTA NP_001032720.1:n.-7_-6delinsTA
NM_005214.4:c.-7_-6delinsTA NP_005205.2:n.-7_-6delinsTA
XR_241294.1:n.134_135delinsTA
NM_001037631.3:c.-7_-6delinsTA NP_001032720.1:n.-7_-6delinsTA
NM_005214.5:c.-7_-6delinsTA MANE Select NP_005205.2:n.-7_-6delinsTA