Canonical Allele Identifier: CA1322149276
Gene: CTLA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203869658T= , CM000664.2:g.203869658T= GRCh38
NC_000002.11:g.204734381T= , CM000664.1:g.204734381T= GRCh37
NC_000002.10:g.204442626T= NCBI36
NG_011502.1:g.6873T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696049.1:c.110-928T= ENSP00000512353.1:n.110-928T=
ENST00000696479.1:c.182-928T= ENSP00000512655.1:n.182-928T=
ENST00000648405.2:c.110-928T= MANE Select ENSP00000497102.1:n.110-928T=
ENST00000295854.10:c.110-928T= ENSP00000295854.6:n.110-928T=
ENST00000302823.7:c.110-928T= ENSP00000303939.3:n.110-928T=
ENST00000472206.1:c.110-928T= ENSP00000417779.1:n.110-928T=
ENST00000487393.1:n.109+1607T=
NM_001037631.2:c.110-928T= NP_001032720.1:n.110-928T=
NM_005214.4:c.110-928T= NP_005205.2:n.110-928T=
XR_241294.1:n.250-928T=
NM_001037631.3:c.110-928T= NP_001032720.1:n.110-928T=
NM_005214.5:c.110-928T= MANE Select NP_005205.2:n.110-928T=