Canonical Allele Identifier: CA2841140844

Gene: TNFRSF1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6333603_6333604del , CM000674.2:g.6333603_6333604del	GRCh38
NC_000012.11:g.6442769_6442770del , CM000674.1:g.6442769_6442770del	GRCh37
NC_000012.10:g.6313030_6313031del	NCBI36
NG_007506.1:g.13493_13494del , LRG_193:g.13493_13494del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.357-87_357-86del
ENST00000437813.8:c.323-87_323-86del	ENSP00000513672.1:n.323-87_323-86del
ENST00000440083.7:c.323-87_323-86del	ENSP00000413224.3:n.323-87_323-86del
ENST00000535958.2:c.*150-87_*150-86del	ENSP00000513673.1:n.*150-87_*150-86del
ENST00000698339.1:c.323-87_323-86del	ENSP00000513670.1:n.323-87_323-86del
ENST00000698340.1:c.323-87_323-86del	ENSP00000513671.1:n.323-87_323-86del
ENST00000162749.7:c.323-87_323-86del MANE Select	ENSP00000162749.2:n.323-87_323-86del
ENST00000162749.6:c.323-87_323-86del	ENSP00000162749.2:n.323-87_323-86del
ENST00000366159.8:c.323-87_323-86del	ENSP00000380389.3:n.323-87_323-86del
ENST00000437813.7:n.284-87_284-86del
ENST00000440083.6:c.323-87_323-86del	ENSP00000413224.2:n.323-87_323-86del
ENST00000534885.5:c.169-87_169-86del	ENSP00000441803.1:n.169-87_169-86del
ENST00000536194.1:c.296-87_296-86del	ENSP00000442919.1:n.296-87_296-86del
ENST00000539372.5:c.323-87_323-86del	ENSP00000442059.1:n.323-87_323-86del
ENST00000540022.5:c.194-87_194-86del	ENSP00000438343.1:n.194-87_194-86del
ENST00000543048.5:c.215-152_215-151del	ENSP00000439981.1:n.215-152_215-151del
ENST00000543995.5:c.194-152_194-151del	ENSP00000442405.1:n.194-152_194-151del
NM_001065.3:c.323-87_323-86del , LRG_193t1:c.323-87_323-86del	NP_001056.1:n.323-87_323-86del
NM_001346091.1:c.-2-87_-2-86del	NP_001333020.1:n.-2-87_-2-86del
NM_001346092.1:c.-255-87_-255-86del	NP_001333021.1:n.-255-87_-255-86del
NR_144351.1:n.626-87_626-86del
NM_001065.4:c.323-87_323-86del MANE Select	NP_001056.1:n.323-87_323-86del
NM_001346091.2:c.-2-87_-2-86del	NP_001333020.1:n.-2-87_-2-86del
NM_001346092.2:c.-255-87_-255-86del	NP_001333021.1:n.-255-87_-255-86del
NR_144351.2:n.585-87_585-86del