Canonical Allele Identifier: CA2662768868

Gene: CTLA4

Linked Data

• gnomAD v4: 2-203871541-T-TCCC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203871542_203871543insCCC , CM000664.2:g.203871542_203871543insCCC	GRCh38
NC_000002.11:g.204736265_204736266insCCC , CM000664.1:g.204736265_204736266insCCC	GRCh37
NC_000002.10:g.204444510_204444511insCCC	NCBI36
NG_011502.1:g.8757_8758insCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696049.1:c.507+115_507+116insCCC	ENSP00000512353.1:n.507+115_507+116insCCC
ENST00000696479.1:c.639+55_639+56insCCC	ENSP00000512655.1:n.639+55_639+56insCCC
ENST00000427473.3:n.491+609_491+610insCCC
ENST00000648405.2:c.567+55_567+56insCCC MANE Select	ENSP00000497102.1:n.567+55_567+56insCCC
ENST00000650075.1:n.591+55_591+56insCCC
ENST00000295854.10:c.457+609_457+610insCCC	ENSP00000295854.6:n.457+609_457+610insCCC
ENST00000302823.7:c.567+55_567+56insCCC	ENSP00000303939.3:n.567+55_567+56insCCC
ENST00000427473.2:c.346+609_346+610insCCC	ENSP00000409707.2:n.346+609_346+610insCCC
ENST00000472206.1:c.172+894_172+895insCCC	ENSP00000417779.1:n.172+894_172+895insCCC
ENST00000487393.1:n.110-1166_110-1165insCCC
NM_001037631.2:c.457+609_457+610insCCC	NP_001032720.1:n.457+609_457+610insCCC
NM_005214.4:c.567+55_567+56insCCC	NP_005205.2:n.567+55_567+56insCCC
XR_241294.1:n.707+55_707+56insCCC
NM_001037631.3:c.457+609_457+610insCCC	NP_001032720.1:n.457+609_457+610insCCC
NM_005214.5:c.567+55_567+56insCCC MANE Select	NP_005205.2:n.567+55_567+56insCCC