Canonical Allele Identifier: CA2662768852

Gene: CTLA4

Linked Data

• gnomAD v4: 2-203871513-ATG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203871515_203871516del , CM000664.2:g.203871515_203871516del	GRCh38
NC_000002.11:g.204736238_204736239del , CM000664.1:g.204736238_204736239del	GRCh37
NC_000002.10:g.204444483_204444484del	NCBI36
NG_011502.1:g.8730_8731del

Transcript Alleles

HGVS	Amino-acid change
ENST00000696049.1:c.507+88_507+89del	ENSP00000512353.1:n.507+88_507+89del
ENST00000696479.1:c.639+28_639+29del	ENSP00000512655.1:n.639+28_639+29del
ENST00000427473.3:n.491+582_491+583del
ENST00000648405.2:c.567+28_567+29del MANE Select	ENSP00000497102.1:n.567+28_567+29del
ENST00000650075.1:n.591+28_591+29del
ENST00000295854.10:c.457+582_457+583del	ENSP00000295854.6:n.457+582_457+583del
ENST00000302823.7:c.567+28_567+29del	ENSP00000303939.3:n.567+28_567+29del
ENST00000427473.2:c.346+582_346+583del	ENSP00000409707.2:n.346+582_346+583del
ENST00000472206.1:c.172+867_172+868del	ENSP00000417779.1:n.172+867_172+868del
ENST00000487393.1:n.110-1193_110-1192del
NM_001037631.2:c.457+582_457+583del	NP_001032720.1:n.457+582_457+583del
NM_005214.4:c.567+28_567+29del	NP_005205.2:n.567+28_567+29del
XR_241294.1:n.707+28_707+29del
NM_001037631.3:c.457+582_457+583del	NP_001032720.1:n.457+582_457+583del
NM_005214.5:c.567+28_567+29del MANE Select	NP_005205.2:n.567+28_567+29del