Canonical Allele Identifier: CA2662768248
Gene: CTLA4 HGNC NCBI

Linked Data

gnomAD v4: 2-203867936-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203867936T>A , CM000664.2:g.203867936T>A GRCh38
NC_000002.11:g.204732659T>A , CM000664.1:g.204732659T>A GRCh37
NC_000002.10:g.204440904T>A NCBI36
NG_011502.1:g.5151T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000696049.1:c.-7T>A ENSP00000512353.1:n.-7T>A
ENST00000696479.1:c.66T>A ENSP00000512655.1:p.His22Gln
ENST00000648405.2:c.-7T>A MANE Select ENSP00000497102.1:n.-7T>A
ENST00000302823.7:c.-7T>A ENSP00000303939.3:n.-7T>A
NM_001037631.2:c.-7T>A NP_001032720.1:n.-7T>A
NM_005214.4:c.-7T>A NP_005205.2:n.-7T>A
XR_241294.1:n.134T>A
NM_001037631.3:c.-7T>A NP_001032720.1:n.-7T>A
NM_005214.5:c.-7T>A MANE Select NP_005205.2:n.-7T>A
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