Canonical Allele Identifier: CA2250304996

Gene: TNFRSF13B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16948917_16948937delinsCAGCTGATGCAGTCCCTCAGG , CM000679.2:g.16948917_16948937delinsCAGCTGATGCAGTCCCTCAGG	GRCh38
NC_000017.10:g.16852231_16852251delinsCAGCTGATGCAGTCCCTCAGG , CM000679.1:g.16852231_16852251delinsCAGCTGATGCAGTCCCTCAGG	GRCh37
NC_000017.9:g.16792956_16792976delinsCAGCTGATGCAGTCCCTCAGG	NCBI36
NG_007281.1:g.28152_28172delinsCCTGAGGGACTGCATCAGCTG , LRG_120:g.28152_28172delinsCCTGAGGGACTGCATCAGCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261652.7:c.246_266delinsCCTGAGGGACTGCATCAGCTG MANE Select	ENSP00000261652.2:p.Leu82=
ENST00000261652.6:c.246_266delinsCCTGAGGGACTGCATCAGCTG	ENSP00000261652.2:p.Leu82=
ENST00000579315.5:c.246_266delinsCCTGAGGGACTGCATCAGCTG	ENSP00000464069.1:p.Leu82=
ENST00000581616.2:n.249_269delinsCCTGAGGGACTGCATCAGCTG
ENST00000582931.5:n.150_170delinsCCTGAGGGACTGCATCAGCTG
ENST00000583789.1:c.108_128delinsCCTGAGGGACTGCATCAGCTG	ENSP00000462952.1:p.Leu36=
ENST00000584950.5:c.108_128delinsCCTGAGGGACTGCATCAGCTG	ENSP00000463582.1:p.Leu36=
NM_012452.2:c.246_266delinsCCTGAGGGACTGCATCAGCTG , LRG_120t1:c.246_266delinsCCTGAGGGACTGCATCAGCTG	NP_036584.1:p.Leu82=
NM_012452.3:c.246_266delinsCCTGAGGGACTGCATCAGCTG MANE Select	NP_036584.1:p.Leu82=