Canonical Allele Identifier: CA2250305473
Gene: TNFRSF13B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16949065_16949068delinsTAAA , CM000679.2:g.16949065_16949068delinsTAAA GRCh38
NC_000017.10:g.16852379_16852382delinsTAAA , CM000679.1:g.16852379_16852382delinsTAAA GRCh37
NC_000017.9:g.16793104_16793107delinsTAAA NCBI36
NG_007281.1:g.28021_28024delinsTTTA , LRG_120:g.28021_28024delinsTTTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000261652.7:c.200-85_200-82delinsTTTA MANE Select ENSP00000261652.2:n.200-85_200-82delinsTTTA
ENST00000261652.6:c.200-85_200-82delinsTTTA ENSP00000261652.2:n.200-85_200-82delinsTTTA
ENST00000579315.5:c.200-85_200-82delinsTTTA ENSP00000464069.1:n.200-85_200-82delinsTTTA
ENST00000581616.2:n.203-85_203-82delinsTTTA
ENST00000582931.5:n.104-85_104-82delinsTTTA
ENST00000583789.1:c.62-85_62-82delinsTTTA ENSP00000462952.1:n.62-85_62-82delinsTTTA
ENST00000584950.5:c.62-85_62-82delinsTTTA ENSP00000463582.1:n.62-85_62-82delinsTTTA
NM_012452.2:c.200-85_200-82delinsTTTA , LRG_120t1:c.200-85_200-82delinsTTTA NP_036584.1:n.200-85_200-82delinsTTTA
NM_012452.3:c.200-85_200-82delinsTTTA MANE Select NP_036584.1:n.200-85_200-82delinsTTTA