Canonical Allele Identifier: CA1322148561
Gene: CTLA4 HGNC NCBI

Linked Data

dbSNP Id: rs1688656064

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203867919C>T , CM000664.2:g.203867919C>T GRCh38
NC_000002.11:g.204732642C>T , CM000664.1:g.204732642C>T GRCh37
NC_000002.10:g.204440887C>T NCBI36
NG_011502.1:g.5134C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000696049.1:c.-24C>T ENSP00000512353.1:n.-24C>T
ENST00000696479.1:c.49C>T ENSP00000512655.1:p.Pro17Ser
ENST00000648405.2:c.-24C>T MANE Select ENSP00000497102.1:n.-24C>T
ENST00000302823.7:c.-24C>T ENSP00000303939.3:n.-24C>T
NM_001037631.2:c.-24C>T NP_001032720.1:n.-24C>T
NM_005214.4:c.-24C>T NP_005205.2:n.-24C>T
XR_241294.1:n.117C>T
NM_001037631.3:c.-24C>T NP_001032720.1:n.-24C>T
NM_005214.5:c.-24C>T MANE Select NP_005205.2:n.-24C>T