Canonical Allele Identifier: CA383547697

Gene: TNFRSF1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330663A>C , CM000674.2:g.6330663A>C	GRCh38
NC_000012.11:g.6439829A>C , CM000674.1:g.6439829A>C	GRCh37
NC_000012.10:g.6310090A>C	NCBI36
NG_007506.1:g.16433T>G , LRG_193:g.16433T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1775T>G
ENST00000437813.8:c.*135T>G	ENSP00000513672.1:n.*135T>G
ENST00000440083.7:c.893T>G	ENSP00000413224.3:p.Leu298Ter
ENST00000535038.2:n.856T>G
ENST00000535958.2:c.*501T>G	ENSP00000513673.1:n.*501T>G
ENST00000698337.1:n.664T>G
ENST00000698338.1:n.1088T>G
ENST00000698339.1:c.*169T>G	ENSP00000513670.1:n.*169T>G
ENST00000698340.1:c.600T>G	ENSP00000513671.1:p.Phe200Leu
ENST00000162749.7:c.674T>G MANE Select	ENSP00000162749.2:p.Leu225Ter
ENST00000162749.6:c.674T>G	ENSP00000162749.2:p.Leu225Ter
ENST00000534885.5:c.*151T>G	ENSP00000441803.1:n.*151T>G
ENST00000535038.1:n.485T>G
ENST00000536717.5:n.578T>G
ENST00000537842.5:n.278T>G
ENST00000539372.5:c.674T>G	ENSP00000442059.1:p.Leu225Ter
ENST00000540022.5:c.545T>G	ENSP00000438343.1:p.Leu182Ter
ENST00000543359.5:n.86T>G
ENST00000543995.5:c.*261T>G	ENSP00000442405.1:n.*261T>G
NM_001065.3:c.674T>G , LRG_193t1:c.674T>G	NP_001056.1:p.Leu225Ter
NM_001346091.1:c.350T>G	NP_001333020.1:p.Leu117Ter
NM_001346092.1:c.215T>G	NP_001333021.1:p.Leu72Ter
NR_144351.1:n.903T>G
NM_001065.4:c.674T>G MANE Select	NP_001056.1:p.Leu225Ter
NM_001346091.2:c.350T>G	NP_001333020.1:p.Leu117Ter
NM_001346092.2:c.215T>G	NP_001333021.1:p.Leu72Ter
NR_144351.2:n.862T>G