Canonical Allele Identifier: CA2753941488
Gene: CTLA4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203867876A>C , CM000664.2:g.203867876A>C GRCh38
NC_000002.11:g.204732599A>C , CM000664.1:g.204732599A>C GRCh37
NC_000002.10:g.204440844A>C NCBI36
NG_011502.1:g.5091A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000696049.1:c.-67A>C ENSP00000512353.1:n.-67A>C
ENST00000696479.1:c.48-42A>C ENSP00000512655.1:n.48-42A>C
ENST00000648405.2:c.-67A>C MANE Select ENSP00000497102.1:n.-67A>C
ENST00000302823.7:c.-67A>C ENSP00000303939.3:n.-67A>C
NM_001037631.2:c.-67A>C NP_001032720.1:n.-67A>C
NM_005214.4:c.-67A>C NP_005205.2:n.-67A>C
XR_241294.1:n.74A>C
NM_001037631.3:c.-67A>C NP_001032720.1:n.-67A>C
NM_005214.5:c.-67A>C MANE Select NP_005205.2:n.-67A>C
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