Canonical Allele Identifier: CA2250292546

Gene: TNFRSF13B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16941543_16941544delinsGC , CM000679.2:g.16941543_16941544delinsGC	GRCh38
NC_000017.10:g.16844857_16844858delinsGC , CM000679.1:g.16844857_16844858delinsGC	GRCh37
NC_000017.9:g.16785582_16785583delinsGC	NCBI36
NG_007281.1:g.35545_35546delinsGC , LRG_120:g.35545_35546delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261652.7:c.446-1033_446-1032delinsGC MANE Select	ENSP00000261652.2:n.446-1033_446-1032delinsGC
ENST00000261652.6:c.446-1033_446-1032delinsGC	ENSP00000261652.2:n.446-1033_446-1032delinsGC
ENST00000579315.5:c.445+7194_445+7195delinsGC	ENSP00000464069.1:n.445+7194_445+7195delinsGC
ENST00000581616.2:n.449-67_449-66delinsGC
ENST00000582931.5:n.349+7194_349+7195delinsGC
ENST00000583789.1:c.308-1033_308-1032delinsGC	ENSP00000462952.1:n.308-1033_308-1032delinsGC
ENST00000584950.5:c.308-1033_308-1032delinsGC	ENSP00000463582.1:n.308-1033_308-1032delinsGC
NM_012452.2:c.446-1033_446-1032delinsGC , LRG_120t1:c.446-1033_446-1032delinsGC	NP_036584.1:n.446-1033_446-1032delinsGC
NM_012452.3:c.446-1033_446-1032delinsGC MANE Select	NP_036584.1:n.446-1033_446-1032delinsGC