Canonical Allele Identifier: CA2577220044
Gene: CTLA4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203867930C>A , CM000664.2:g.203867930C>A GRCh38
NC_000002.11:g.204732653C>A , CM000664.1:g.204732653C>A GRCh37
NC_000002.10:g.204440898C>A NCBI36
NG_011502.1:g.5145C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000696049.1:c.-13C>A ENSP00000512353.1:n.-13C>A
ENST00000696479.1:c.60C>A ENSP00000512655.1:p.Arg20=
ENST00000648405.2:c.-13C>A MANE Select ENSP00000497102.1:n.-13C>A
ENST00000302823.7:c.-13C>A ENSP00000303939.3:n.-13C>A
NM_001037631.2:c.-13C>A NP_001032720.1:n.-13C>A
NM_005214.4:c.-13C>A NP_005205.2:n.-13C>A
XR_241294.1:n.128C>A
NM_001037631.3:c.-13C>A NP_001032720.1:n.-13C>A
NM_005214.5:c.-13C>A MANE Select NP_005205.2:n.-13C>A