Canonical Allele Identifier: CA6405331

Gene: TNFRSF1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6329948C>G , CM000674.2:g.6329948C>G	GRCh38
NC_000012.11:g.6439114C>G , CM000674.1:g.6439114C>G	GRCh37
NC_000012.10:g.6309375C>G	NCBI36
NG_007506.1:g.17148G>C , LRG_193:g.17148G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001065.4:c.887G>C MANE Select	NP_001056.1:p.Ser296Thr
ENST00000162749.7:c.887G>C MANE Select	ENSP00000162749.2:p.Ser296Thr
NM_001065.3:c.887G>C , LRG_193t1:c.887G>C	NP_001056.1:p.Ser296Thr
NM_001346091.1:c.563G>C	NP_001333020.1:p.Ser188Thr
NM_001346091.2:c.563G>C	NP_001333020.1:p.Ser188Thr
NM_001346092.1:c.428G>C	NP_001333021.1:p.Ser143Thr
NM_001346092.2:c.428G>C	NP_001333021.1:p.Ser143Thr
NR_144351.1:n.1116G>C
NR_144351.2:n.1075G>C
ENST00000162749.6:c.887G>C	ENSP00000162749.2:p.Ser296Thr
ENST00000366159.9:n.1988G>C
ENST00000437813.8:c.*348G>C	ENSP00000513672.1:n.*348G>C
ENST00000440083.7:c.1106G>C	ENSP00000413224.3:p.Ser369Thr
ENST00000534885.5:c.*364G>C	ENSP00000441803.1:n.*364G>C
ENST00000535958.2:c.*714G>C	ENSP00000513673.1:n.*714G>C
ENST00000536717.5:n.791G>C
ENST00000537842.5:n.373-49G>C
ENST00000540022.5:c.758G>C	ENSP00000438343.1:p.Ser253Thr
ENST00000543359.5:n.299G>C
ENST00000543995.5:c.*474G>C	ENSP00000442405.1:n.*474G>C
ENST00000698337.1:n.848G>C
ENST00000698338.1:n.1501G>C
ENST00000698339.1:c.*382G>C	ENSP00000513670.1:n.*382G>C
ENST00000698340.1:c.*126G>C	ENSP00000513671.1:n.*126G>C