Canonical Allele Identifier: CA350138829

Gene: CTLA4

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203870926T>G , CM000664.2:g.203870926T>G	GRCh38
NC_000002.11:g.204735649T>G , CM000664.1:g.204735649T>G	GRCh37
NC_000002.10:g.204443894T>G	NCBI36
NG_011502.1:g.8141T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_005214.5:c.450T>G MANE Select	NP_005205.2:p.Tyr150Ter
ENST00000648405.2:c.450T>G MANE Select	ENSP00000497102.1:p.Tyr150Ter
NM_001037631.2:c.450T>G	NP_001032720.1:p.Tyr150Ter
NM_001037631.3:c.450T>G	NP_001032720.1:p.Tyr150Ter
NM_005214.4:c.450T>G	NP_005205.2:p.Tyr150Ter
ENST00000295854.10:c.450T>G	ENSP00000295854.6:p.Tyr150Ter
ENST00000302823.7:c.450T>G	ENSP00000303939.3:p.Tyr150Ter
ENST00000427473.2:c.339T>G	ENSP00000409707.2:p.Tyr113Ter
ENST00000427473.3:n.484T>G
ENST00000472206.1:c.172+278T>G	ENSP00000417779.1:n.172+278T>G
ENST00000487393.1:n.110-1782T>G
ENST00000650075.1:n.474T>G
ENST00000696049.1:c.450T>G	ENSP00000512353.1:p.Tyr150Ter
ENST00000696479.1:c.522T>G	ENSP00000512655.1:p.Tyr174Ter
XR_241294.1:n.590T>G