Canonical Allele Identifier: CA2617250622
Gene: TNFRSF1A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6330605_6330616del , CM000674.2:g.6330605_6330616del GRCh38
NC_000012.11:g.6439771_6439782del , CM000674.1:g.6439771_6439782del GRCh37
NC_000012.10:g.6310032_6310043del NCBI36
NG_007506.1:g.16484_16495del , LRG_193:g.16484_16495del

Transcript Alleles

HGVS Amino-acid Change
ENST00000366159.9:n.1826_1837del
ENST00000437813.8:c.*186_*197del ENSP00000513672.1:n.*186_*197del
ENST00000440083.7:c.944_955del ENSP00000413224.3:p.Lys315_Ser318del
ENST00000535038.2:n.907_918del
ENST00000535958.2:c.*552_*563del ENSP00000513673.1:n.*552_*563del
ENST00000698337.1:n.715_726del
ENST00000698338.1:n.1139_1150del
ENST00000698339.1:c.*220_*231del ENSP00000513670.1:n.*220_*231del
ENST00000698340.1:c.651_662del ENSP00000513671.1:p.Gln217_Leu220del
ENST00000162749.7:c.725_736del MANE Select ENSP00000162749.2:p.Lys242_Ser245del
ENST00000162749.6:c.725_736del ENSP00000162749.2:p.Lys242_Ser245del
ENST00000534885.5:c.*202_*213del ENSP00000441803.1:n.*202_*213del
ENST00000535038.1:n.536_547del
ENST00000536717.5:n.629_640del
ENST00000537842.5:n.329_340del
ENST00000539372.5:c.725_736del ENSP00000442059.1:p.Lys242_Ser245del
ENST00000540022.5:c.596_607del ENSP00000438343.1:p.Lys199_Ser202del
ENST00000543359.5:n.137_148del
ENST00000543995.5:c.*312_*323del ENSP00000442405.1:n.*312_*323del
NM_001065.3:c.725_736del , LRG_193t1:c.725_736del NP_001056.1:p.Lys242_Ser245del
NM_001346091.1:c.401_412del NP_001333020.1:p.Lys134_Ser137del
NM_001346092.1:c.266_277del NP_001333021.1:p.Lys89_Ser92del
NR_144351.1:n.954_965del
NM_001065.4:c.725_736del MANE Select NP_001056.1:p.Lys242_Ser245del
NM_001346091.2:c.401_412del NP_001333020.1:p.Lys134_Ser137del
NM_001346092.2:c.266_277del NP_001333021.1:p.Lys89_Ser92del
NR_144351.2:n.913_924del