Canonical Allele Identifier: CA645516073

Gene: CTLA4

Linked Data

• gnomAD v4: 2-203871442-GT-G
• COSMIC: COSM2908690

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203871449del , CM000664.2:g.203871449del	GRCh38
NC_000002.11:g.204736172del , CM000664.1:g.204736172del	GRCh37
NC_000002.10:g.204444417del	NCBI36
NG_011502.1:g.8664del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696049.1:c.507+22del	ENSP00000512353.1:n.507+22del
ENST00000696479.1:c.601del	ENSP00000512655.1:p.Tyr201IlefsTer10
ENST00000427473.3:n.491+516del
ENST00000648405.2:c.529del MANE Select	ENSP00000497102.1:p.Tyr177IlefsTer10
ENST00000650075.1:n.553del
ENST00000295854.10:c.457+516del	ENSP00000295854.6:n.457+516del
ENST00000302823.7:c.529del	ENSP00000303939.3:p.Tyr177IlefsTer10
ENST00000427473.2:c.346+516del	ENSP00000409707.2:n.346+516del
ENST00000472206.1:c.172+801del	ENSP00000417779.1:n.172+801del
ENST00000487393.1:n.110-1259del
NM_001037631.2:c.457+516del	NP_001032720.1:n.457+516del
NM_005214.4:c.529del	NP_005205.2:p.Tyr177IlefsTer10
XR_241294.1:n.669del
NM_001037631.3:c.457+516del	NP_001032720.1:n.457+516del
NM_005214.5:c.529del MANE Select	NP_005205.2:p.Tyr177IlefsTer10