Canonical Allele Identifier: CA2541300414

Gene: TNFRSF1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330828_6330831del , CM000674.2:g.6330828_6330831del	GRCh38
NC_000012.11:g.6439994_6439997del , CM000674.1:g.6439994_6439997del	GRCh37
NC_000012.10:g.6310255_6310258del	NCBI36
NG_007506.1:g.16265_16268del , LRG_193:g.16265_16268del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1726+22_1726+25del
ENST00000437813.8:c.*86+22_*86+25del	ENSP00000513672.1:n.*86+22_*86+25del
ENST00000440083.7:c.844+22_844+25del	ENSP00000413224.3:n.844+22_844+25del
ENST00000535038.2:n.807+22_807+25del
ENST00000535958.2:c.*452+22_*452+25del	ENSP00000513673.1:n.*452+22_*452+25del
ENST00000698337.1:n.496_499del
ENST00000698338.1:n.920_923del
ENST00000698339.1:c.*120+22_*120+25del	ENSP00000513670.1:n.*120+22_*120+25del
ENST00000698340.1:c.552-120_552-117del	ENSP00000513671.1:n.552-120_552-117del
ENST00000162749.7:c.625+22_625+25del MANE Select	ENSP00000162749.2:n.625+22_625+25del
ENST00000162749.6:c.625+22_625+25del	ENSP00000162749.2:n.625+22_625+25del
ENST00000534885.5:c.*102+22_*102+25del	ENSP00000441803.1:n.*102+22_*102+25del
ENST00000535038.1:n.317_320del
ENST00000536717.5:n.529+22_529+25del
ENST00000537842.5:n.229+22_229+25del
ENST00000539372.5:c.625+22_625+25del	ENSP00000442059.1:n.625+22_625+25del
ENST00000540022.5:c.496+22_496+25del	ENSP00000438343.1:n.496+22_496+25del
ENST00000543359.5:n.38-120_38-117del
ENST00000543995.5:c.*212+22_*212+25del	ENSP00000442405.1:n.*212+22_*212+25del
NM_001065.3:c.625+22_625+25del , LRG_193t1:c.625+22_625+25del	NP_001056.1:n.625+22_625+25del
NM_001346091.1:c.301+22_301+25del	NP_001333020.1:n.301+22_301+25del
NM_001346092.1:c.166+22_166+25del	NP_001333021.1:n.166+22_166+25del
NR_144351.1:n.855-120_855-117del
NM_001065.4:c.625+22_625+25del MANE Select	NP_001056.1:n.625+22_625+25del
NM_001346091.2:c.301+22_301+25del	NP_001333020.1:n.301+22_301+25del
NM_001346092.2:c.166+22_166+25del	NP_001333021.1:n.166+22_166+25del
NR_144351.2:n.814-120_814-117del