Canonical Allele Identifier: CA1322154004
Gene: CTLA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203871510A= , CM000664.2:g.203871510A= GRCh38
NC_000002.11:g.204736233A= , CM000664.1:g.204736233A= GRCh37
NC_000002.10:g.204444478A= NCBI36
NG_011502.1:g.8725A=

Transcript Alleles

HGVS Amino-acid change
ENST00000696049.1:c.507+83A= ENSP00000512353.1:n.507+83A=
ENST00000696479.1:c.639+23A= ENSP00000512655.1:n.639+23A=
ENST00000427473.3:n.491+577A=
ENST00000648405.2:c.567+23A= MANE Select ENSP00000497102.1:n.567+23A=
ENST00000650075.1:n.591+23A=
ENST00000295854.10:c.457+577A= ENSP00000295854.6:n.457+577A=
ENST00000302823.7:c.567+23A= ENSP00000303939.3:n.567+23A=
ENST00000427473.2:c.346+577A= ENSP00000409707.2:n.346+577A=
ENST00000472206.1:c.172+862A= ENSP00000417779.1:n.172+862A=
ENST00000487393.1:n.110-1198A=
NM_001037631.2:c.457+577A= NP_001032720.1:n.457+577A=
NM_005214.4:c.567+23A= NP_005205.2:n.567+23A=
XR_241294.1:n.707+23A=
NM_001037631.3:c.457+577A= NP_001032720.1:n.457+577A=
NM_005214.5:c.567+23A= MANE Select NP_005205.2:n.567+23A=