Canonical Allele Identifier: CA2753941551

Gene: CTLA4

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203871140_203871218del , CM000664.2:g.203871140_203871218del	GRCh38
NC_000002.11:g.204735863_204735941del , CM000664.1:g.204735863_204735941del	GRCh37
NC_000002.10:g.204444108_204444186del	NCBI36
NG_011502.1:g.8355_8433del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696049.1:c.457+207_458-160del	ENSP00000512353.1:n.457+207_458-160del
ENST00000696479.1:c.529+207_530-160del	ENSP00000512655.1:n.529+207_530-160del
ENST00000427473.3:n.491+207_491+285del
ENST00000648405.2:c.457+207_458-160del MANE Select	ENSP00000497102.1:n.457+207_458-160del
ENST00000650075.1:n.481+207_482-160del
ENST00000295854.10:c.457+207_457+285del	ENSP00000295854.6:n.457+207_457+285del
ENST00000302823.7:c.457+207_458-160del	ENSP00000303939.3:n.457+207_458-160del
ENST00000427473.2:c.346+207_346+285del	ENSP00000409707.2:n.346+207_346+285del
ENST00000472206.1:c.172+492_172+570del	ENSP00000417779.1:n.172+492_172+570del
ENST00000487393.1:n.110-1568_110-1490del
NM_001037631.2:c.457+207_457+285del	NP_001032720.1:n.457+207_457+285del
NM_005214.4:c.457+207_458-160del	NP_005205.2:n.457+207_458-160del
XR_241294.1:n.597+207_598-160del
NM_001037631.3:c.457+207_457+285del	NP_001032720.1:n.457+207_457+285del
NM_005214.5:c.457+207_458-160del MANE Select	NP_005205.2:n.457+207_458-160del