Canonical Allele Identifier: CA2535986211

Gene: TNFRSF13B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16941528_16941529insTTTTGGGATAA , CM000679.2:g.16941528_16941529insTTTTGGGATAA	GRCh38
NC_000017.10:g.16844842_16844843insTTTTGGGATAA , CM000679.1:g.16844842_16844843insTTTTGGGATAA	GRCh37
NC_000017.9:g.16785567_16785568insTTTTGGGATAA	NCBI36
NG_007281.1:g.35560_35561insTTATCCCAAAA , LRG_120:g.35560_35561insTTATCCCAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261652.7:c.446-1018_446-1017insTTATCCCAAAA MANE Select	ENSP00000261652.2:n.446-1018_446-1017insTTATCCCAAAA
ENST00000261652.6:c.446-1018_446-1017insTTATCCCAAAA	ENSP00000261652.2:n.446-1018_446-1017insTTATCCCAAAA
ENST00000579315.5:c.445+7209_445+7210insTTATCCCAAAA	ENSP00000464069.1:n.445+7209_445+7210insTTATCCCAAAA
ENST00000581616.2:n.449-52_449-51insTTATCCCAAAA
ENST00000582931.5:n.349+7209_349+7210insTTATCCCAAAA
ENST00000583789.1:c.308-1018_308-1017insTTATCCCAAAA	ENSP00000462952.1:n.308-1018_308-1017insTTATCCCAAAA
ENST00000584950.5:c.308-1018_308-1017insTTATCCCAAAA	ENSP00000463582.1:n.308-1018_308-1017insTTATCCCAAAA
NM_012452.2:c.446-1018_446-1017insTTATCCCAAAA , LRG_120t1:c.446-1018_446-1017insTTATCCCAAAA	NP_036584.1:n.446-1018_446-1017insTTATCCCAAAA
NM_012452.3:c.446-1018_446-1017insTTATCCCAAAA MANE Select	NP_036584.1:n.446-1018_446-1017insTTATCCCAAAA