Canonical Allele Identifier: CA1322150082

Gene: CTLA4

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203871405_203871406delinsTC , CM000664.2:g.203871405_203871406delinsTC	GRCh38
NC_000002.11:g.204736128_204736129delinsTC , CM000664.1:g.204736128_204736129delinsTC	GRCh37
NC_000002.10:g.204444373_204444374delinsTC	NCBI36
NG_011502.1:g.8620_8621delinsTC

Transcript Alleles

HGVS	Amino-acid change
ENST00000696049.1:c.485_486delinsTC	ENSP00000512353.1:p.Phe162=
ENST00000696479.1:c.557_558delinsTC	ENSP00000512655.1:p.Phe186=
ENST00000427473.3:n.491+472_491+473delinsTC
ENST00000648405.2:c.485_486delinsTC MANE Select	ENSP00000497102.1:p.Phe162=
ENST00000650075.1:n.509_510delinsTC
ENST00000295854.10:c.457+472_457+473delinsTC	ENSP00000295854.6:n.457+472_457+473delins...
ENST00000302823.7:c.485_486delinsTC	ENSP00000303939.3:p.Phe162=
ENST00000427473.2:c.346+472_346+473delinsTC	ENSP00000409707.2:n.346+472_346+473delins...
ENST00000472206.1:c.172+757_172+758delinsTC	ENSP00000417779.1:n.172+757_172+758delins...
ENST00000487393.1:n.110-1303_110-1302delinsTC
NM_001037631.2:c.457+472_457+473delinsTC	NP_001032720.1:n.457+472_457+473delinsTC
NM_005214.4:c.485_486delinsTC	NP_005205.2:p.Phe162=
XR_241294.1:n.625_626delinsTC
NM_001037631.3:c.457+472_457+473delinsTC	NP_001032720.1:n.457+472_457+473delinsTC
NM_005214.5:c.485_486delinsTC MANE Select	NP_005205.2:p.Phe162=