Canonical Allele Identifier: CA2250292552

Gene: TNFRSF13B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16941545_16941546delinsCG , CM000679.2:g.16941545_16941546delinsCG	GRCh38
NC_000017.10:g.16844859_16844860delinsCG , CM000679.1:g.16844859_16844860delinsCG	GRCh37
NC_000017.9:g.16785584_16785585delinsCG	NCBI36
NG_007281.1:g.35543_35544delinsCG , LRG_120:g.35543_35544delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261652.7:c.446-1035_446-1034delinsCG MANE Select	ENSP00000261652.2:n.446-1035_446-1034delinsCG
ENST00000261652.6:c.446-1035_446-1034delinsCG	ENSP00000261652.2:n.446-1035_446-1034delinsCG
ENST00000579315.5:c.445+7192_445+7193delinsCG	ENSP00000464069.1:n.445+7192_445+7193delinsCG
ENST00000581616.2:n.449-69_449-68delinsCG
ENST00000582931.5:n.349+7192_349+7193delinsCG
ENST00000583789.1:c.308-1035_308-1034delinsCG	ENSP00000462952.1:n.308-1035_308-1034delinsCG
ENST00000584950.5:c.308-1035_308-1034delinsCG	ENSP00000463582.1:n.308-1035_308-1034delinsCG
NM_012452.2:c.446-1035_446-1034delinsCG , LRG_120t1:c.446-1035_446-1034delinsCG	NP_036584.1:n.446-1035_446-1034delinsCG
NM_012452.3:c.446-1035_446-1034delinsCG MANE Select	NP_036584.1:n.446-1035_446-1034delinsCG