Canonical Allele Identifier: CA126974
Gene: CTLA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 16921
dbSNP Id: rs231775

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203867991A>G , CM000664.2:g.203867991A>G GRCh38
NC_000002.11:g.204732714A>G , CM000664.1:g.204732714A>G GRCh37
NC_000002.10:g.204440959A>G NCBI36
NG_011502.1:g.5206A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000696049.1:c.49A>G ENSP00000512353.1:p.Thr17Ala
ENST00000696479.1:c.121A>G ENSP00000512655.1:p.Thr41Ala
ENST00000648405.2:c.49A>G MANE Select ENSP00000497102.1:p.Thr17Ala
ENST00000295854.10:c.49A>G ENSP00000295854.6:p.Thr17Ala
ENST00000302823.7:c.49A>G ENSP00000303939.3:p.Thr17Ala
ENST00000472206.1:c.49A>G ENSP00000417779.1:p.Thr17Ala
ENST00000487393.1:n.49A>G
NM_001037631.2:c.49A>G NP_001032720.1:p.Thr17Ala
NM_005214.4:c.49A>G NP_005205.2:p.Thr17Ala
XR_241294.1:n.189A>G
NM_001037631.3:c.49A>G NP_001032720.1:p.Thr17Ala
NM_005214.5:c.49A>G MANE Select NP_005205.2:p.Thr17Ala