Canonical Allele Identifier: CA2695224526

Gene: TNFRSF13B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16948876_16948877del , CM000679.2:g.16948876_16948877del	GRCh38
NC_000017.10:g.16852190_16852191del , CM000679.1:g.16852190_16852191del	GRCh37
NC_000017.9:g.16792915_16792916del	NCBI36
NG_007281.1:g.28212_28213del , LRG_120:g.28212_28213del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261652.7:c.306_307del MANE Select	ENSP00000261652.2:p.Phe103LeufsTer2
ENST00000261652.6:c.306_307del	ENSP00000261652.2:p.Phe103LeufsTer2
ENST00000579315.5:c.306_307del	ENSP00000464069.1:p.Phe103LeufsTer2
ENST00000581616.2:n.309_310del
ENST00000582931.5:n.210_211del
ENST00000583789.1:c.168_169del	ENSP00000462952.1:p.Phe57LeufsTer2
ENST00000584950.5:c.168_169del	ENSP00000463582.1:p.Phe57LeufsTer2
NM_012452.2:c.306_307del , LRG_120t1:c.306_307del	NP_036584.1:p.Phe103LeufsTer2
NM_012452.3:c.306_307del MANE Select	NP_036584.1:p.Phe103LeufsTer2