Canonical Allele Identifier: CA2662768919

Gene: CTLA4

Linked Data

• gnomAD v4: 2-203871615-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203871615G>T , CM000664.2:g.203871615G>T	GRCh38
NC_000002.11:g.204736338G>T , CM000664.1:g.204736338G>T	GRCh37
NC_000002.10:g.204444583G>T	NCBI36
NG_011502.1:g.8830G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696049.1:c.507+188G>T	ENSP00000512353.1:n.507+188G>T
ENST00000696479.1:c.639+128G>T	ENSP00000512655.1:n.639+128G>T
ENST00000427473.3:n.491+682G>T
ENST00000648405.2:c.567+128G>T MANE Select	ENSP00000497102.1:n.567+128G>T
ENST00000650075.1:n.591+128G>T
ENST00000295854.10:c.457+682G>T	ENSP00000295854.6:n.457+682G>T
ENST00000302823.7:c.567+128G>T	ENSP00000303939.3:n.567+128G>T
ENST00000427473.2:c.346+682G>T	ENSP00000409707.2:n.346+682G>T
ENST00000472206.1:c.172+967G>T	ENSP00000417779.1:n.172+967G>T
ENST00000487393.1:n.110-1093G>T
NM_001037631.2:c.457+682G>T	NP_001032720.1:n.457+682G>T
NM_005214.4:c.567+128G>T	NP_005205.2:n.567+128G>T
XR_241294.1:n.707+128G>T
NM_001037631.3:c.457+682G>T	NP_001032720.1:n.457+682G>T
NM_005214.5:c.567+128G>T MANE Select	NP_005205.2:n.567+128G>T