Canonical Allele Identifier: CA1322154101

Gene: CTLA4

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203871605_203871606delinsAG , CM000664.2:g.203871605_203871606delinsAG	GRCh38
NC_000002.11:g.204736328_204736329delinsAG , CM000664.1:g.204736328_204736329delinsAG	GRCh37
NC_000002.10:g.204444573_204444574delinsAG	NCBI36
NG_011502.1:g.8820_8821delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696049.1:c.507+178_507+179delinsAG	ENSP00000512353.1:n.507+178_507+179delinsAG
ENST00000696479.1:c.639+118_639+119delinsAG	ENSP00000512655.1:n.639+118_639+119delinsAG
ENST00000427473.3:n.491+672_491+673delinsAG
ENST00000648405.2:c.567+118_567+119delinsAG MANE Select	ENSP00000497102.1:n.567+118_567+119delinsAG
ENST00000650075.1:n.591+118_591+119delinsAG
ENST00000295854.10:c.457+672_457+673delinsAG	ENSP00000295854.6:n.457+672_457+673delinsAG
ENST00000302823.7:c.567+118_567+119delinsAG	ENSP00000303939.3:n.567+118_567+119delinsAG
ENST00000427473.2:c.346+672_346+673delinsAG	ENSP00000409707.2:n.346+672_346+673delinsAG
ENST00000472206.1:c.172+957_172+958delinsAG	ENSP00000417779.1:n.172+957_172+958delinsAG
ENST00000487393.1:n.110-1103_110-1102delinsAG
NM_001037631.2:c.457+672_457+673delinsAG	NP_001032720.1:n.457+672_457+673delinsAG
NM_005214.4:c.567+118_567+119delinsAG	NP_005205.2:n.567+118_567+119delinsAG
XR_241294.1:n.707+118_707+119delinsAG
NM_001037631.3:c.457+672_457+673delinsAG	NP_001032720.1:n.457+672_457+673delinsAG
NM_005214.5:c.567+118_567+119delinsAG MANE Select	NP_005205.2:n.567+118_567+119delinsAG