Canonical Allele Identifier: CA2577220125

Gene: CTLA4

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203871328del , CM000664.2:g.203871328del	GRCh38
NC_000002.11:g.204736051del , CM000664.1:g.204736051del	GRCh37
NC_000002.10:g.204444296del	NCBI36
NG_011502.1:g.8543del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696049.1:c.458-50del	ENSP00000512353.1:n.458-50del
ENST00000696479.1:c.530-50del	ENSP00000512655.1:n.530-50del
ENST00000427473.3:n.491+395del
ENST00000648405.2:c.458-50del MANE Select	ENSP00000497102.1:n.458-50del
ENST00000650075.1:n.482-50del
ENST00000295854.10:c.457+395del	ENSP00000295854.6:n.457+395del
ENST00000302823.7:c.458-50del	ENSP00000303939.3:n.458-50del
ENST00000427473.2:c.346+395del	ENSP00000409707.2:n.346+395del
ENST00000472206.1:c.172+680del	ENSP00000417779.1:n.172+680del
ENST00000487393.1:n.110-1380del
NM_001037631.2:c.457+395del	NP_001032720.1:n.457+395del
NM_005214.4:c.458-50del	NP_005205.2:n.458-50del
XR_241294.1:n.598-50del
NM_001037631.3:c.457+395del	NP_001032720.1:n.457+395del
NM_005214.5:c.458-50del MANE Select	NP_005205.2:n.458-50del