Canonical Allele Identifier: CA645657115
Gene: TNFRSF1B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.12208442_12208443insA , CM000663.2:g.12208442_12208443insA GRCh38
NC_000001.10:g.12268499_12268500insA , CM000663.1:g.12268499_12268500insA GRCh37
NC_000001.9:g.12191086_12191087insA NCBI36
NG_029791.1:g.46440_46441insA

Transcript Alleles

HGVS Amino-acid change
ENST00000376259.7:c.*1422_*1423insA MANE Select ENSP00000365435.3:n.*1422_*1423insA
ENST00000376259.6:c.*1422_*1423insA ENSP00000365435.3:n.*1422_*1423insA
ENST00000492361.1:n.2797_2798insA
NM_001066.2:c.*1422_*1423insA NP_001057.1:n.*1422_*1423insA
XM_011542060.1:c.*1422_*1423insA XP_011540362.1:n.*1422_*1423insA
XM_011542061.1:c.*1422_*1423insA XP_011540363.1:n.*1422_*1423insA
XM_011542062.1:c.2856_2857insA XP_011540364.1:n.2856_2857insA
XM_011542063.1:c.*1422_*1423insA XP_011540365.1:n.*1422_*1423insA
XM_011542060.2:c.*1422_*1423insA XP_011540362.1:n.*1422_*1423insA
XM_011542063.2:c.*1422_*1423insA XP_011540365.1:n.*1422_*1423insA
XM_017002214.1:c.*1422_*1423insA XP_016857703.1:n.*1422_*1423insA
XM_017002215.1:c.*1422_*1423insA XP_016857704.1:n.*1422_*1423insA
NM_001066.3:c.*1422_*1423insA MANE Select NP_001057.1:n.*1422_*1423insA