Canonical Allele Identifier: CA2250292482

Gene: TNFRSF13B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16941508_16941540delinsAGATGACACGTCAAGAAGAGCGAGTCCCACTTC , CM000679.2:g.16941508_16941540delinsAGATGACACGTCAAGAAGAGCGAGTCCCACTTC	GRCh38
NC_000017.10:g.16844822_16844854delinsAGATGACACGTCAAGAAGAGCGAGTCCCACTTC , CM000679.1:g.16844822_16844854delinsAGATGACACGTCAAGAAGAGCGAGTCCCACTTC	GRCh37
NC_000017.9:g.16785547_16785579delinsAGATGACACGTCAAGAAGAGCGAGTCCCACTTC	NCBI36
NG_007281.1:g.35549_35581delinsGAAGTGGGACTCGCTCTTCTTGACGTGTCATCT , LRG_120:g.35549_35581delinsGAAGTGGGACTCGCTCTTCTTGACGTGTCATCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261652.7:c.446-1029_446-997delinsGAAGTGGGACTCGCTCTTCTTGACGTGTCATCT MANE Select	ENSP00000261652.2:n.446-1029_446-997delinsGAAGTGGGACTCGCTCTTC...
ENST00000261652.6:c.446-1029_446-997delinsGAAGTGGGACTCGCTCTTCTTGACGTGTCATCT	ENSP00000261652.2:n.446-1029_446-997delinsGAAGTGGGACTCGCTCTTC...
ENST00000579315.5:c.445+7198_445+7230delinsGAAGTGGGACTCGCTCTTCTTGACGTGTCATCT	ENSP00000464069.1:n.445+7198_445+7230delinsGAAGTGGGACTCGCTCTT...
ENST00000581616.2:n.449-63_449-31delinsGAAGTGGGACTCGCTCTTCTTGACGTGTCATCT
ENST00000582931.5:n.349+7198_349+7230delinsGAAGTGGGACTCGCTCTTCTTGACGTGTCATCT
ENST00000583789.1:c.308-1029_308-997delinsGAAGTGGGACTCGCTCTTCTTGACGTGTCATCT	ENSP00000462952.1:n.308-1029_308-997delinsGAAGTGGGACTCGCTCTTC...
ENST00000584950.5:c.308-1029_308-997delinsGAAGTGGGACTCGCTCTTCTTGACGTGTCATCT	ENSP00000463582.1:n.308-1029_308-997delinsGAAGTGGGACTCGCTCTTC...
NM_012452.2:c.446-1029_446-997delinsGAAGTGGGACTCGCTCTTCTTGACGTGTCATCT , LRG_120t1:c.446-1029_446-997delinsGAAGTGGGACTCGCTCTTCTTGACGTGTCATCT	NP_036584.1:n.446-1029_446-997delinsGAAGTGGGACTCGCTCTTCTTGACG...
NM_012452.3:c.446-1029_446-997delinsGAAGTGGGACTCGCTCTTCTTGACGTGTCATCT MANE Select	NP_036584.1:n.446-1029_446-997delinsGAAGTGGGACTCGCTCTTCTTGACG...