Canonical Allele Identifier: CA2014026545

Gene: TNFRSF1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6334536_6334538delinsGCT , CM000674.2:g.6334536_6334538delinsGCT	GRCh38
NC_000012.11:g.6443702_6443704delinsGCT , CM000674.1:g.6443702_6443704delinsGCT	GRCh37
NC_000012.10:g.6313963_6313965delinsGCT	NCBI36
NG_007506.1:g.12558_12560delinsAGC , LRG_193:g.12558_12560delinsAGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.74-294_74-292delinsAGC
ENST00000437813.8:c.40-294_40-292delinsAGC	ENSP00000513672.1:n.40-294_40-292delinsAGC
ENST00000440083.7:c.40-294_40-292delinsAGC	ENSP00000413224.3:n.40-294_40-292delinsAGC
ENST00000535958.2:c.40-294_40-292delinsAGC	ENSP00000513673.1:n.40-294_40-292delinsAGC
ENST00000698339.1:c.40-294_40-292delinsAGC	ENSP00000513670.1:n.40-294_40-292delinsAGC
ENST00000698340.1:c.40-294_40-292delinsAGC	ENSP00000513671.1:n.40-294_40-292delinsAGC
ENST00000162749.7:c.40-294_40-292delinsAGC MANE Select	ENSP00000162749.2:n.40-294_40-292delinsAGC
ENST00000162749.6:c.40-294_40-292delinsAGC	ENSP00000162749.2:n.40-294_40-292delinsAGC
ENST00000366159.8:c.40-294_40-292delinsAGC	ENSP00000380389.3:n.40-294_40-292delinsAGC
ENST00000440083.6:c.40-294_40-292delinsAGC	ENSP00000413224.2:n.40-294_40-292delinsAGC
ENST00000534885.5:c.40-673_40-671delinsAGC	ENSP00000441803.1:n.40-673_40-671delinsAGC
ENST00000535958.1:n.261-294_261-292delinsAGC
ENST00000536194.1:c.40-294_40-292delinsAGC	ENSP00000442919.1:n.40-294_40-292delinsAGC
ENST00000538363.1:n.230-294_230-292delinsAGC
ENST00000539372.5:c.40-294_40-292delinsAGC	ENSP00000442059.1:n.40-294_40-292delinsAGC
ENST00000540022.5:c.40-294_40-292delinsAGC	ENSP00000438343.1:n.40-294_40-292delinsAGC
ENST00000543048.5:c.40-294_40-292delinsAGC	ENSP00000439981.1:n.40-294_40-292delinsAGC
ENST00000543995.5:c.40-294_40-292delinsAGC	ENSP00000442405.1:n.40-294_40-292delinsAGC
NM_001065.3:c.40-294_40-292delinsAGC , LRG_193t1:c.40-294_40-292delinsAGC	NP_001056.1:n.40-294_40-292delinsAGC
NM_001346091.1:c.-131-673_-131-671delinsAGC	NP_001333020.1:n.-131-673_-131-671delinsAGC
NM_001346092.1:c.-538-294_-538-292delinsAGC	NP_001333021.1:n.-538-294_-538-292delinsAGC
NR_144351.1:n.343-294_343-292delinsAGC
NM_001065.4:c.40-294_40-292delinsAGC MANE Select	NP_001056.1:n.40-294_40-292delinsAGC
NM_001346091.2:c.-131-673_-131-671delinsAGC	NP_001333020.1:n.-131-673_-131-671delinsAGC
NM_001346092.2:c.-538-294_-538-292delinsAGC	NP_001333021.1:n.-538-294_-538-292delinsAGC
NR_144351.2:n.302-294_302-292delinsAGC