Canonical Allele Identifier: CA350138739
Community Standard Title: NM_005214.5(CTLA4):c.410C>A (p.Pro137Gln)
Gene: CTLA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203870886C>A , CM000664.2:g.203870886C>A GRCh38
NC_000002.11:g.204735609C>A , CM000664.1:g.204735609C>A GRCh37
NC_000002.10:g.204443854C>A NCBI36
NG_011502.1:g.8101C>A

Transcript Alleles

HGVS Amino-acid Change
NM_005214.5:c.410C>A MANE Select NP_005205.2:p.Pro137Gln
ENST00000648405.2:c.410C>A MANE Select ENSP00000497102.1:p.Pro137Gln
NM_001037631.2:c.410C>A NP_001032720.1:p.Pro137Gln
NM_001037631.3:c.410C>A NP_001032720.1:p.Pro137Gln
NM_005214.4:c.410C>A NP_005205.2:p.Pro137Gln
ENST00000295854.10:c.410C>A ENSP00000295854.6:p.Pro137Gln
ENST00000302823.7:c.410C>A ENSP00000303939.3:p.Pro137Gln
ENST00000427473.2:c.299C>A ENSP00000409707.2:p.Pro100Gln
ENST00000427473.3:n.444C>A
ENST00000472206.1:c.172+238C>A ENSP00000417779.1:n.172+238C>A
ENST00000487393.1:n.110-1822C>A
ENST00000650075.1:n.434C>A
ENST00000696049.1:c.410C>A ENSP00000512353.1:p.Pro137Gln
ENST00000696479.1:c.482C>A ENSP00000512655.1:p.Pro161Gln
XR_241294.1:n.550C>A