Canonical Allele Identifier: CA645613802
Gene: CD40LG HGNC NCBI

Linked Data

COSMIC: COSM150916

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659178_136659205del , CM000685.2:g.136659178_136659205del GRCh38
NC_000023.10:g.135741337_135741364del , CM000685.1:g.135741337_135741364del GRCh37
NC_000023.9:g.135569003_135569030del NCBI36
NG_007280.1:g.16002_16029del , LRG_141:g.16002_16029del

Transcript Alleles

HGVS Amino-acid Change
ENST00000695724.1:c.*167_*194del ENSP00000512122.1:n.*167_*194del
ENST00000695725.1:c.*104_*131del ENSP00000512123.1:n.*104_*131del
ENST00000695726.1:n.2517_2544del
ENST00000695729.1:n.3352_3379del
ENST00000370629.7:c.549_576del MANE Select ENSP00000359663.2:p.Ser185AlafsTer2
ENST00000370628.2:c.486_513del ENSP00000359662.2:p.Ser164AlafsTer2
ENST00000370629.6:c.549_576del ENSP00000359663.2:p.Ser185AlafsTer2
NM_000074.2:c.549_576del , LRG_141t1:c.549_576del NP_000065.1:p.Ser185AlafsTer2
NM_000074.3:c.549_576del MANE Select NP_000065.1:p.Ser185AlafsTer2