Canonical Allele Identifier: CA1322148577
Gene: CTLA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203867943A= , CM000664.2:g.203867943A= GRCh38
NC_000002.11:g.204732666A= , CM000664.1:g.204732666A= GRCh37
NC_000002.10:g.204440911A= NCBI36
NG_011502.1:g.5158A=

Transcript Alleles

HGVS Amino-acid change
ENST00000696049.1:c.1A= ENSP00000512353.1:p.Met1=
ENST00000696479.1:c.73A= ENSP00000512655.1:p.Met25=
ENST00000648405.2:c.1A= MANE Select ENSP00000497102.1:p.Met1=
ENST00000295854.10:c.1A= ENSP00000295854.6:p.Met1=
ENST00000302823.7:c.1A= ENSP00000303939.3:p.Met1=
ENST00000472206.1:c.1A= ENSP00000417779.1:p.Met1=
ENST00000487393.1:n.1A=
NM_001037631.2:c.1A= NP_001032720.1:p.Met1=
NM_005214.4:c.1A= NP_005205.2:p.Met1=
XR_241294.1:n.141A=
NM_001037631.3:c.1A= NP_001032720.1:p.Met1=
NM_005214.5:c.1A= MANE Select NP_005205.2:p.Met1=