Canonical Allele Identifier: CA2662768239
Gene: CTLA4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203867922G>T , CM000664.2:g.203867922G>T GRCh38
NC_000002.11:g.204732645G>T , CM000664.1:g.204732645G>T GRCh37
NC_000002.10:g.204440890G>T NCBI36
NG_011502.1:g.5137G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000696049.1:c.-21G>T ENSP00000512353.1:n.-21G>T
ENST00000696479.1:c.52G>T ENSP00000512655.1:p.Glu18Ter
ENST00000648405.2:c.-21G>T MANE Select ENSP00000497102.1:n.-21G>T
ENST00000302823.7:c.-21G>T ENSP00000303939.3:n.-21G>T
NM_001037631.2:c.-21G>T NP_001032720.1:n.-21G>T
NM_005214.4:c.-21G>T NP_005205.2:n.-21G>T
XR_241294.1:n.120G>T
NM_001037631.3:c.-21G>T NP_001032720.1:n.-21G>T
NM_005214.5:c.-21G>T MANE Select NP_005205.2:n.-21G>T