Canonical Allele Identifier: CA981911063
Gene: TNFRSF13B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16948713_16948714insTTGCCTTGGGTGGCTTACCTGGACTTGCAAACCTGCGTGACACCAG , CM000679.2:g.16948713_16948714insTTGCCTTGGGTGGCTTACCTGGACTTGCAAACCTGCGTGACACCAG GRCh38
NC_000017.10:g.16852027_16852028insTTGCCTTGGGTGGCTTACCTGGACTTGCAAACCTGCGTGACACCAG , CM000679.1:g.16852027_16852028insTTGCCTTGGGTGGCTTACCTGGACTTGCAAACCTGCGTGACACCAG GRCh37
NC_000017.9:g.16792752_16792753insTTGCCTTGGGTGGCTTACCTGGACTTGCAAACCTGCGTGACACCAG NCBI36
NG_007281.1:g.28375_28376insCTGGTGTCACGCAGGTTTGCAAGTCCAGGTAAGCCACCCAAGGCAA , LRG_120:g.28375_28376insCTGGTGTCACGCAGGTTTGCAAGTCCAGGTAAGCCACCCAAGGCAA

Transcript Alleles

HGVS Amino-acid change
ENST00000261652.7:c.445+24_445+25insCTGGTGTCACGCAGGTTTGCAAGTCCAGGTAAGCCACCCAAGGCAA MANE Select ENSP00000261652.2:n.445+24_445+25insCTGGTGTCACGCAGGTTTGCAAGTC...
ENST00000261652.6:c.445+24_445+25insCTGGTGTCACGCAGGTTTGCAAGTCCAGGTAAGCCACCCAAGGCAA ENSP00000261652.2:n.445+24_445+25insCTGGTGTCACGCAGGTTTGCAAGTC...
ENST00000579315.5:c.445+24_445+25insCTGGTGTCACGCAGGTTTGCAAGTCCAGGTAAGCCACCCAAGGCAA ENSP00000464069.1:n.445+24_445+25insCTGGTGTCACGCAGGTTTGCAAGTC...
ENST00000581616.2:n.448+24_448+25insCTGGTGTCACGCAGGTTTGCAAGTCCAGGTAAGCCACCCAAGGCAA
ENST00000582931.5:n.349+24_349+25insCTGGTGTCACGCAGGTTTGCAAGTCCAGGTAAGCCACCCAAGGCAA
ENST00000583789.1:c.307+24_307+25insCTGGTGTCACGCAGGTTTGCAAGTCCAGGTAAGCCACCCAAGGCAA ENSP00000462952.1:n.307+24_307+25insCTGGTGTCACGCAGGTTTGCAAGTC...
ENST00000584950.5:c.307+24_307+25insCTGGTGTCACGCAGGTTTGCAAGTCCAGGTAAGCCACCCAAGGCAA ENSP00000463582.1:n.307+24_307+25insCTGGTGTCACGCAGGTTTGCAAGTC...
NM_012452.2:c.445+24_445+25insCTGGTGTCACGCAGGTTTGCAAGTCCAGGTAAGCCACCCAAGGCAA , LRG_120t1:c.445+24_445+25insCTGGTGTCACGCAGGTTTGCAAGTCCAGGTAAGCCACCCAAGGCAA NP_036584.1:n.445+24_445+25insCTGGTGTCACGCAGGTTTGCAAGTCCAGGTA...
NM_012452.3:c.445+24_445+25insCTGGTGTCACGCAGGTTTGCAAGTCCAGGTAAGCCACCCAAGGCAA MANE Select NP_036584.1:n.445+24_445+25insCTGGTGTCACGCAGGTTTGCAAGTCCAGGTA...