Canonical Allele Identifier: CA2808628609

Gene: TNFRSF13B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16941648_16941649insG , CM000679.2:g.16941648_16941649insG	GRCh38
NC_000017.10:g.16844962_16844963insG , CM000679.1:g.16844962_16844963insG	GRCh37
NC_000017.9:g.16785687_16785688insG	NCBI36
NG_007281.1:g.35440_35441insC , LRG_120:g.35440_35441insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261652.7:c.446-1138_446-1137insC MANE Select	ENSP00000261652.2:n.446-1138_446-1137insC
ENST00000261652.6:c.446-1138_446-1137insC	ENSP00000261652.2:n.446-1138_446-1137insC
ENST00000579315.5:c.445+7089_445+7090insC	ENSP00000464069.1:n.445+7089_445+7090insC
ENST00000581616.2:n.449-172_449-171insC
ENST00000582931.5:n.349+7089_349+7090insC
ENST00000583789.1:c.308-1138_308-1137insC	ENSP00000462952.1:n.308-1138_308-1137insC
ENST00000584950.5:c.308-1138_308-1137insC	ENSP00000463582.1:n.308-1138_308-1137insC
NM_012452.2:c.446-1138_446-1137insC , LRG_120t1:c.446-1138_446-1137insC	NP_036584.1:n.446-1138_446-1137insC
NM_012452.3:c.446-1138_446-1137insC MANE Select	NP_036584.1:n.446-1138_446-1137insC