Canonical Allele Identifier: CA414756735
Gene: CD40LG HGNC NCBI

Linked Data

gnomAD v4: X-136659342-T-C
MyVariant Identifiers: chrX:g.135741501T>C (hg19) chrX:g.136659342T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659342T>C , CM000685.2:g.136659342T>C GRCh38
NC_000023.10:g.135741501T>C , CM000685.1:g.135741501T>C GRCh37
NC_000023.9:g.135569167T>C NCBI36
NG_007280.1:g.16166T>C , LRG_141:g.16166T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000695724.1:c.*331T>C ENSP00000512122.1:n.*331T>C
ENST00000695725.1:c.*268T>C ENSP00000512123.1:n.*268T>C
ENST00000695726.1:n.2681T>C
ENST00000695729.1:n.3516T>C
ENST00000370629.7:c.713T>C MANE Select ENSP00000359663.2:p.Phe238Ser
ENST00000370628.2:c.650T>C ENSP00000359662.2:p.Phe217Ser
ENST00000370629.6:c.713T>C ENSP00000359663.2:p.Phe238Ser
NM_000074.2:c.713T>C , LRG_141t1:c.713T>C NP_000065.1:p.Phe238Ser
NM_000074.3:c.713T>C MANE Select NP_000065.1:p.Phe238Ser
Search 100 bp 5'
Search 100 bp 3'