Canonical Allele Identifier: CA2695236799

Gene: CD40LG

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136659338_136659339insC , CM000685.2:g.136659338_136659339insC	GRCh38
NC_000023.10:g.135741497_135741498insC , CM000685.1:g.135741497_135741498insC	GRCh37
NC_000023.9:g.135569163_135569164insC	NCBI36
NG_007280.1:g.16162_16163insC , LRG_141:g.16162_16163insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695724.1:c.*327_*328insC	ENSP00000512122.1:n.*327_*328insC
ENST00000695725.1:c.*264_*265insC	ENSP00000512123.1:n.*264_*265insC
ENST00000695726.1:n.2677_2678insC
ENST00000695729.1:n.3512_3513insC
ENST00000370629.7:c.709_710insC MANE Select	ENSP00000359663.2:p.Val237AlafsTer7
ENST00000370628.2:c.646_647insC	ENSP00000359662.2:p.Val216AlafsTer7
ENST00000370629.6:c.709_710insC	ENSP00000359663.2:p.Val237AlafsTer7
NM_000074.2:c.709_710insC , LRG_141t1:c.709_710insC	NP_000065.1:p.Val237AlafsTer7
NM_000074.3:c.709_710insC MANE Select	NP_000065.1:p.Val237AlafsTer7