Canonical Allele Identifier: CA2662768203
Gene: CTLA4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203867830C>T , CM000664.2:g.203867830C>T GRCh38
NC_000002.11:g.204732553C>T , CM000664.1:g.204732553C>T GRCh37
NC_000002.10:g.204440798C>T NCBI36
NG_011502.1:g.5045C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000696049.1:c.-113C>T ENSP00000512353.1:n.-113C>T
ENST00000696479.1:c.48-88C>T ENSP00000512655.1:n.48-88C>T
ENST00000648405.2:c.-113C>T MANE Select ENSP00000497102.1:n.-113C>T
ENST00000302823.7:c.-113C>T ENSP00000303939.3:n.-113C>T
NM_001037631.2:c.-113C>T NP_001032720.1:n.-113C>T
NM_005214.4:c.-113C>T NP_005205.2:n.-113C>T
XR_241294.1:n.28C>T
NM_001037631.3:c.-113C>T NP_001032720.1:n.-113C>T
NM_005214.5:c.-113C>T MANE Select NP_005205.2:n.-113C>T