Canonical Allele Identifier: CA2662768810

Gene: CTLA4

Linked Data

• gnomAD v4: 2-203871304-TCACCAA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203871305_203871310del , CM000664.2:g.203871305_203871310del	GRCh38
NC_000002.11:g.204736028_204736033del , CM000664.1:g.204736028_204736033del	GRCh37
NC_000002.10:g.204444273_204444278del	NCBI36
NG_011502.1:g.8520_8525del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696049.1:c.458-73_458-68del	ENSP00000512353.1:n.458-73_458-68del
ENST00000696479.1:c.530-73_530-68del	ENSP00000512655.1:n.530-73_530-68del
ENST00000427473.3:n.491+372_491+377del
ENST00000648405.2:c.458-73_458-68del MANE Select	ENSP00000497102.1:n.458-73_458-68del
ENST00000650075.1:n.482-73_482-68del
ENST00000295854.10:c.457+372_457+377del	ENSP00000295854.6:n.457+372_457+377del
ENST00000302823.7:c.458-73_458-68del	ENSP00000303939.3:n.458-73_458-68del
ENST00000427473.2:c.346+372_346+377del	ENSP00000409707.2:n.346+372_346+377del
ENST00000472206.1:c.172+657_172+662del	ENSP00000417779.1:n.172+657_172+662del
ENST00000487393.1:n.110-1403_110-1398del
NM_001037631.2:c.457+372_457+377del	NP_001032720.1:n.457+372_457+377del
NM_005214.4:c.458-73_458-68del	NP_005205.2:n.458-73_458-68del
XR_241294.1:n.598-73_598-68del
NM_001037631.3:c.457+372_457+377del	NP_001032720.1:n.457+372_457+377del
NM_005214.5:c.458-73_458-68del MANE Select	NP_005205.2:n.458-73_458-68del