Canonical Allele Identifier: CA2014027989

Gene: TNFRSF1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6337602_6337603delinsAC , CM000674.2:g.6337602_6337603delinsAC	GRCh38
NC_000012.11:g.6446768_6446769delinsAC , CM000674.1:g.6446768_6446769delinsAC	GRCh37
NC_000012.10:g.6317029_6317030delinsAC	NCBI36
NG_007506.1:g.9493_9494delinsGT , LRG_193:g.9493_9494delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.74-3359_74-3358delinsGT
ENST00000437813.8:c.40-3359_40-3358delinsGT	ENSP00000513672.1:n.40-3359_40-3358delinsGT
ENST00000440083.7:c.40-3359_40-3358delinsGT	ENSP00000413224.3:n.40-3359_40-3358delinsGT
ENST00000535958.2:c.40-3359_40-3358delinsGT	ENSP00000513673.1:n.40-3359_40-3358delinsGT
ENST00000698339.1:c.40-3359_40-3358delinsGT	ENSP00000513670.1:n.40-3359_40-3358delinsGT
ENST00000698340.1:c.40-3359_40-3358delinsGT	ENSP00000513671.1:n.40-3359_40-3358delinsGT
ENST00000162749.7:c.40-3359_40-3358delinsGT MANE Select	ENSP00000162749.2:n.40-3359_40-3358delinsGT
ENST00000162749.6:c.40-3359_40-3358delinsGT	ENSP00000162749.2:n.40-3359_40-3358delinsGT
ENST00000366159.8:c.40-3359_40-3358delinsGT	ENSP00000380389.3:n.40-3359_40-3358delinsGT
ENST00000440083.6:c.40-3359_40-3358delinsGT	ENSP00000413224.2:n.40-3359_40-3358delinsGT
ENST00000534885.5:c.40-3738_40-3737delinsGT	ENSP00000441803.1:n.40-3738_40-3737delinsGT
ENST00000535958.1:n.261-3359_261-3358delinsGT
ENST00000536194.1:c.40-3359_40-3358delinsGT	ENSP00000442919.1:n.40-3359_40-3358delinsGT
ENST00000538363.1:n.230-3359_230-3358delinsGT
ENST00000539372.5:c.40-3359_40-3358delinsGT	ENSP00000442059.1:n.40-3359_40-3358delinsGT
ENST00000540022.5:c.40-3359_40-3358delinsGT	ENSP00000438343.1:n.40-3359_40-3358delinsGT
ENST00000543048.5:c.40-3359_40-3358delinsGT	ENSP00000439981.1:n.40-3359_40-3358delinsGT
ENST00000543995.5:c.40-3359_40-3358delinsGT	ENSP00000442405.1:n.40-3359_40-3358delinsGT
NM_001065.3:c.40-3359_40-3358delinsGT , LRG_193t1:c.40-3359_40-3358delinsGT	NP_001056.1:n.40-3359_40-3358delinsGT
NM_001346091.1:c.-131-3738_-131-3737delinsGT	NP_001333020.1:n.-131-3738_-131-3737delinsGT
NM_001346092.1:c.-538-3359_-538-3358delinsGT	NP_001333021.1:n.-538-3359_-538-3358delinsGT
NR_144351.1:n.343-3359_343-3358delinsGT
NM_001065.4:c.40-3359_40-3358delinsGT MANE Select	NP_001056.1:n.40-3359_40-3358delinsGT
NM_001346091.2:c.-131-3738_-131-3737delinsGT	NP_001333020.1:n.-131-3738_-131-3737delinsGT
NM_001346092.2:c.-538-3359_-538-3358delinsGT	NP_001333021.1:n.-538-3359_-538-3358delinsGT
NR_144351.2:n.302-3359_302-3358delinsGT