Canonical Allele Identifier: CA1322148532
Gene: CTLA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203867829G= , CM000664.2:g.203867829G= GRCh38
NC_000002.11:g.204732552G= , CM000664.1:g.204732552G= GRCh37
NC_000002.10:g.204440797G= NCBI36
NG_011502.1:g.5044G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696049.1:c.-114G= ENSP00000512353.1:n.-114G=
ENST00000696479.1:c.48-89G= ENSP00000512655.1:n.48-89G=
ENST00000648405.2:c.-114G= MANE Select ENSP00000497102.1:n.-114G=
ENST00000302823.7:c.-114G= ENSP00000303939.3:n.-114G=
NM_001037631.2:c.-114G= NP_001032720.1:n.-114G=
NM_005214.4:c.-114G= NP_005205.2:n.-114G=
XR_241294.1:n.27G=
NM_001037631.3:c.-114G= NP_001032720.1:n.-114G=
NM_005214.5:c.-114G= MANE Select NP_005205.2:n.-114G=