Canonical Allele Identifier: CA2841140843

Gene: TNFRSF1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6333587C>A , CM000674.2:g.6333587C>A	GRCh38
NC_000012.11:g.6442753C>A , CM000674.1:g.6442753C>A	GRCh37
NC_000012.10:g.6313014C>A	NCBI36
NG_007506.1:g.13509G>T , LRG_193:g.13509G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.357-71G>T
ENST00000437813.8:c.323-71G>T	ENSP00000513672.1:n.323-71G>T
ENST00000440083.7:c.323-71G>T	ENSP00000413224.3:n.323-71G>T
ENST00000535958.2:c.*150-71G>T	ENSP00000513673.1:n.*150-71G>T
ENST00000698339.1:c.323-71G>T	ENSP00000513670.1:n.323-71G>T
ENST00000698340.1:c.323-71G>T	ENSP00000513671.1:n.323-71G>T
ENST00000162749.7:c.323-71G>T MANE Select	ENSP00000162749.2:n.323-71G>T
ENST00000162749.6:c.323-71G>T	ENSP00000162749.2:n.323-71G>T
ENST00000366159.8:c.323-71G>T	ENSP00000380389.3:n.323-71G>T
ENST00000437813.7:n.284-71G>T
ENST00000440083.6:c.323-71G>T	ENSP00000413224.2:n.323-71G>T
ENST00000534885.5:c.169-71G>T	ENSP00000441803.1:n.169-71G>T
ENST00000536194.1:c.296-71G>T	ENSP00000442919.1:n.296-71G>T
ENST00000539372.5:c.323-71G>T	ENSP00000442059.1:n.323-71G>T
ENST00000540022.5:c.194-71G>T	ENSP00000438343.1:n.194-71G>T
ENST00000543048.5:c.215-136G>T	ENSP00000439981.1:n.215-136G>T
ENST00000543995.5:c.194-136G>T	ENSP00000442405.1:n.194-136G>T
NM_001065.3:c.323-71G>T , LRG_193t1:c.323-71G>T	NP_001056.1:n.323-71G>T
NM_001346091.1:c.-2-71G>T	NP_001333020.1:n.-2-71G>T
NM_001346092.1:c.-255-71G>T	NP_001333021.1:n.-255-71G>T
NR_144351.1:n.626-71G>T
NM_001065.4:c.323-71G>T MANE Select	NP_001056.1:n.323-71G>T
NM_001346091.2:c.-2-71G>T	NP_001333020.1:n.-2-71G>T
NM_001346092.2:c.-255-71G>T	NP_001333021.1:n.-255-71G>T
NR_144351.2:n.585-71G>T