Canonical Allele Identifier: CA63786547

Gene: CTLA4

Linked Data

• dbSNP Id: rs767672792
• gnomAD v2: 2-204733989-CTT-C
• gnomAD v3: 2-203869266-CTT-C
• gnomAD v4: 2-203869266-CTT-C
• MyVariant Identifiers: chr2:g.204733990_204733991del (hg19) ; chr2:g.203869267_203869268del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203869268_203869269del , CM000664.2:g.203869268_203869269del	GRCh38
NC_000002.11:g.204733991_204733992del , CM000664.1:g.204733991_204733992del	GRCh37
NC_000002.10:g.204442236_204442237del	NCBI36
NG_011502.1:g.6483_6484del

Transcript Alleles

HGVS	Amino-acid change
ENST00000696049.1:c.109+1217_109+1218del	ENSP00000512353.1:n.109+1217_109+1218del
ENST00000696479.1:c.181+1217_181+1218del	ENSP00000512655.1:n.181+1217_181+1218del
ENST00000648405.2:c.109+1217_109+1218del MANE Select	ENSP00000497102.1:n.109+1217_109+1218del
ENST00000295854.10:c.109+1217_109+1218del	ENSP00000295854.6:n.109+1217_109+1218del
ENST00000302823.7:c.109+1217_109+1218del	ENSP00000303939.3:n.109+1217_109+1218del
ENST00000472206.1:c.109+1217_109+1218del	ENSP00000417779.1:n.109+1217_109+1218del
ENST00000487393.1:n.109+1217_109+1218del
NM_001037631.2:c.109+1217_109+1218del	NP_001032720.1:n.109+1217_109+1218del
NM_005214.4:c.109+1217_109+1218del	NP_005205.2:n.109+1217_109+1218del
XR_241294.1:n.249+1217_249+1218del
NM_001037631.3:c.109+1217_109+1218del	NP_001032720.1:n.109+1217_109+1218del
NM_005214.5:c.109+1217_109+1218del MANE Select	NP_005205.2:n.109+1217_109+1218del