Canonical Allele Identifier: CA1322149199
Gene: CTLA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203869459G= , CM000664.2:g.203869459G= GRCh38
NC_000002.11:g.204734182G= , CM000664.1:g.204734182G= GRCh37
NC_000002.10:g.204442427G= NCBI36
NG_011502.1:g.6674G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696049.1:c.110-1127G= ENSP00000512353.1:n.110-1127G=
ENST00000696479.1:c.182-1127G= ENSP00000512655.1:n.182-1127G=
ENST00000648405.2:c.110-1127G= MANE Select ENSP00000497102.1:n.110-1127G=
ENST00000295854.10:c.110-1127G= ENSP00000295854.6:n.110-1127G=
ENST00000302823.7:c.110-1127G= ENSP00000303939.3:n.110-1127G=
ENST00000472206.1:c.110-1127G= ENSP00000417779.1:n.110-1127G=
ENST00000487393.1:n.109+1408G=
NM_001037631.2:c.110-1127G= NP_001032720.1:n.110-1127G=
NM_005214.4:c.110-1127G= NP_005205.2:n.110-1127G=
XR_241294.1:n.250-1127G=
NM_001037631.3:c.110-1127G= NP_001032720.1:n.110-1127G=
NM_005214.5:c.110-1127G= MANE Select NP_005205.2:n.110-1127G=