Canonical Allele Identifier: CA2250305110

Gene: TNFRSF13B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16948951_16948956delinsACTTGC , CM000679.2:g.16948951_16948956delinsACTTGC	GRCh38
NC_000017.10:g.16852265_16852270delinsACTTGC , CM000679.1:g.16852265_16852270delinsACTTGC	GRCh37
NC_000017.9:g.16792990_16792995delinsACTTGC	NCBI36
NG_007281.1:g.28133_28138delinsGCAAGT , LRG_120:g.28133_28138delinsGCAAGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261652.7:c.227_232delinsGCAAGT MANE Select	ENSP00000261652.2:p.Gly76=
ENST00000261652.6:c.227_232delinsGCAAGT	ENSP00000261652.2:p.Gly76=
ENST00000579315.5:c.227_232delinsGCAAGT	ENSP00000464069.1:p.Gly76=
ENST00000581616.2:n.230_235delinsGCAAGT
ENST00000582931.5:n.131_136delinsGCAAGT
ENST00000583789.1:c.89_94delinsGCAAGT	ENSP00000462952.1:p.Gly30=
ENST00000584950.5:c.89_94delinsGCAAGT	ENSP00000463582.1:p.Gly30=
NM_012452.2:c.227_232delinsGCAAGT , LRG_120t1:c.227_232delinsGCAAGT	NP_036584.1:p.Gly76=
NM_012452.3:c.227_232delinsGCAAGT MANE Select	NP_036584.1:p.Gly76=