Canonical Allele Identifier: CA2725529497

Gene: TNFRSF1A

Linked Data

• dbSNP Id: rs2136817888

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330940_6330941insACACTCGTTTTCTC , CM000674.2:g.6330940_6330941insACACTCGTTTTCTC	GRCh38
NC_000012.11:g.6440106_6440107insACACTCGTTTTCTC , CM000674.1:g.6440106_6440107insACACTCGTTTTCTC	GRCh37
NC_000012.10:g.6310367_6310368insACACTCGTTTTCTC	NCBI36
NG_007506.1:g.16156_16157insAGAAAACGAGTGTG , LRG_193:g.16156_16157insAGAAAACGAGTGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1639_1640insAGAAAACGAGTGTG
ENST00000437813.8:c.*13-14_*13-13insAGAAAACGAGTGTG	ENSP00000513672.1:n.*13-14_*13-13insAGAAAACGAGTGTG
ENST00000440083.7:c.771-14_771-13insAGAAAACGAGTGTG	ENSP00000413224.3:n.771-14_771-13insAGAAAACGAGTGTG
ENST00000535038.2:n.720_721insAGAAAACGAGTGTG
ENST00000535958.2:c.*379-14_*379-13insAGAAAACGAGTGTG	ENSP00000513673.1:n.*379-14_*379-13insAGAAAACGAGTGTG
ENST00000698337.1:n.387_388insAGAAAACGAGTGTG
ENST00000698338.1:n.811_812insAGAAAACGAGTGTG
ENST00000698339.1:c.*33_*34insAGAAAACGAGTGTG	ENSP00000513670.1:n.*33_*34insAGAAAACGAGTGTG
ENST00000698340.1:c.552-229_552-228insAGAAAACGAGTGTG	ENSP00000513671.1:n.552-229_552-228insAGAAAACGAGTGTG
ENST00000162749.7:c.552-14_552-13insAGAAAACGAGTGTG MANE Select	ENSP00000162749.2:n.552-14_552-13insAGAAAACGAGTGTG
ENST00000162749.6:c.552-14_552-13insAGAAAACGAGTGTG	ENSP00000162749.2:n.552-14_552-13insAGAAAACGAGTGTG
ENST00000534885.5:c.*29-14_*29-13insAGAAAACGAGTGTG	ENSP00000441803.1:n.*29-14_*29-13insAGAAAACGAGTGTG
ENST00000535038.1:n.208_209insAGAAAACGAGTGTG
ENST00000536717.5:n.442_443insAGAAAACGAGTGTG
ENST00000537842.5:n.156-14_156-13insAGAAAACGAGTGTG
ENST00000539372.5:c.552-14_552-13insAGAAAACGAGTGTG	ENSP00000442059.1:n.552-14_552-13insAGAAAACGAGTGTG
ENST00000540022.5:c.423-14_423-13insAGAAAACGAGTGTG	ENSP00000438343.1:n.423-14_423-13insAGAAAACGAGTGTG
ENST00000543359.5:n.38-229_38-228insAGAAAACGAGTGTG
ENST00000543995.5:c.*139-14_*139-13insAGAAAACGAGTGTG	ENSP00000442405.1:n.*139-14_*139-13insAGAAAACGAGTGTG
NM_001065.3:c.552-14_552-13insAGAAAACGAGTGTG , LRG_193t1:c.552-14_552-13insAGAAAACGAGTGTG	NP_001056.1:n.552-14_552-13insAGAAAACGAGTGTG
NM_001346091.1:c.228-14_228-13insAGAAAACGAGTGTG	NP_001333020.1:n.228-14_228-13insAGAAAACGAGTGTG
NM_001346092.1:c.93-14_93-13insAGAAAACGAGTGTG	NP_001333021.1:n.93-14_93-13insAGAAAACGAGTGTG
NR_144351.1:n.855-229_855-228insAGAAAACGAGTGTG
NM_001065.4:c.552-14_552-13insAGAAAACGAGTGTG MANE Select	NP_001056.1:n.552-14_552-13insAGAAAACGAGTGTG
NM_001346091.2:c.228-14_228-13insAGAAAACGAGTGTG	NP_001333020.1:n.228-14_228-13insAGAAAACGAGTGTG
NM_001346092.2:c.93-14_93-13insAGAAAACGAGTGTG	NP_001333021.1:n.93-14_93-13insAGAAAACGAGTGTG
NR_144351.2:n.814-229_814-228insAGAAAACGAGTGTG