Canonical Allele Identifier: CA2794414727

Gene: TNFRSF1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330757C>G , CM000674.2:g.6330757C>G	GRCh38
NC_000012.11:g.6439923C>G , CM000674.1:g.6439923C>G	GRCh37
NC_000012.10:g.6310184C>G	NCBI36
NG_007506.1:g.16339G>C , LRG_193:g.16339G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1727-46G>C
ENST00000437813.8:c.*87-46G>C	ENSP00000513672.1:n.*87-46G>C
ENST00000440083.7:c.845-46G>C	ENSP00000413224.3:n.845-46G>C
ENST00000535038.2:n.808-46G>C
ENST00000535958.2:c.*453-46G>C	ENSP00000513673.1:n.*453-46G>C
ENST00000698337.1:n.570G>C
ENST00000698338.1:n.994G>C
ENST00000698339.1:c.*121-46G>C	ENSP00000513670.1:n.*121-46G>C
ENST00000698340.1:c.552-46G>C	ENSP00000513671.1:n.552-46G>C
ENST00000162749.7:c.626-46G>C MANE Select	ENSP00000162749.2:n.626-46G>C
ENST00000162749.6:c.626-46G>C	ENSP00000162749.2:n.626-46G>C
ENST00000534885.5:c.*103-46G>C	ENSP00000441803.1:n.*103-46G>C
ENST00000535038.1:n.391G>C
ENST00000536717.5:n.530-46G>C
ENST00000537842.5:n.230-46G>C
ENST00000539372.5:c.626-46G>C	ENSP00000442059.1:n.626-46G>C
ENST00000540022.5:c.497-46G>C	ENSP00000438343.1:n.497-46G>C
ENST00000543359.5:n.38-46G>C
ENST00000543995.5:c.*213-46G>C	ENSP00000442405.1:n.*213-46G>C
NM_001065.3:c.626-46G>C , LRG_193t1:c.626-46G>C	NP_001056.1:n.626-46G>C
NM_001346091.1:c.302-46G>C	NP_001333020.1:n.302-46G>C
NM_001346092.1:c.167-46G>C	NP_001333021.1:n.167-46G>C
NR_144351.1:n.855-46G>C
NM_001065.4:c.626-46G>C MANE Select	NP_001056.1:n.626-46G>C
NM_001346091.2:c.302-46G>C	NP_001333020.1:n.302-46G>C
NM_001346092.2:c.167-46G>C	NP_001333021.1:n.167-46G>C
NR_144351.2:n.814-46G>C