LDH info

Canonical Allele Identifier: CA173994
Gene: CTLA4 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 161110
ClinVar RCV Id: RCV000148291
dbSNP Id: rs606231418

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203868017del , CM000664.2:g.203868017del GRCh38
NC_000002.11:g.204732740del , CM000664.1:g.204732740del GRCh37
NC_000002.10:g.204440985del NCBI36
NG_011502.1:g.5232del

Transcript Alleles

HGVS Amino-acid change
NM_001037631.2:c.75del VV NP_001032720.1:p.Leu28PhefsTer?
NM_005214.4:c.75del VV NP_005205.2:p.Leu28PhefsTer?
XR_241294.1:n.215del
NM_001037631.3:c.75del VV NP_001032720.1:p.Leu28PhefsTer?
NM_005214.5:c.75del VV MANE Preferred NP_005205.2:p.Leu28PhefsTer?
ENST00000295854.10:n.75del ENSP00000295854.6:p.Leu28PhefsTer?
ENST00000302823.7:c.75del ENSP00000303939.3:p.Leu28PhefsTer?
ENST00000472206.1:n.75del ENSP00000417779.1:p.Leu28PhefsTer?
ENST00000487393.1:n.75del