Canonical Allele Identifier: CA2014024116

Gene: TNFRSF1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330763_6330767delinsGGATA , CM000674.2:g.6330763_6330767delinsGGATA	GRCh38
NC_000012.11:g.6439929_6439933delinsGGATA , CM000674.1:g.6439929_6439933delinsGGATA	GRCh37
NC_000012.10:g.6310190_6310194delinsGGATA	NCBI36
NG_007506.1:g.16329_16333delinsTATCC , LRG_193:g.16329_16333delinsTATCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1727-56_1727-52delinsTATCC
ENST00000437813.8:c.*87-56_*87-52delinsTATCC	ENSP00000513672.1:n.*87-56_*87-52delinsTATCC
ENST00000440083.7:c.845-56_845-52delinsTATCC	ENSP00000413224.3:n.845-56_845-52delinsTATCC
ENST00000535038.2:n.808-56_808-52delinsTATCC
ENST00000535958.2:c.*453-56_*453-52delinsTATCC	ENSP00000513673.1:n.*453-56_*453-52delinsTATCC
ENST00000698337.1:n.560_564delinsTATCC
ENST00000698338.1:n.984_988delinsTATCC
ENST00000698339.1:c.*121-56_*121-52delinsTATCC	ENSP00000513670.1:n.*121-56_*121-52delinsTATCC
ENST00000698340.1:c.552-56_552-52delinsTATCC	ENSP00000513671.1:n.552-56_552-52delinsTATCC
ENST00000162749.7:c.626-56_626-52delinsTATCC MANE Select	ENSP00000162749.2:n.626-56_626-52delinsTATCC
ENST00000162749.6:c.626-56_626-52delinsTATCC	ENSP00000162749.2:n.626-56_626-52delinsTATCC
ENST00000534885.5:c.*103-56_*103-52delinsTATCC	ENSP00000441803.1:n.*103-56_*103-52delinsTATCC
ENST00000535038.1:n.381_385delinsTATCC
ENST00000536717.5:n.530-56_530-52delinsTATCC
ENST00000537842.5:n.230-56_230-52delinsTATCC
ENST00000539372.5:c.626-56_626-52delinsTATCC	ENSP00000442059.1:n.626-56_626-52delinsTATCC
ENST00000540022.5:c.497-56_497-52delinsTATCC	ENSP00000438343.1:n.497-56_497-52delinsTATCC
ENST00000543359.5:n.38-56_38-52delinsTATCC
ENST00000543995.5:c.*213-56_*213-52delinsTATCC	ENSP00000442405.1:n.*213-56_*213-52delinsTATCC
NM_001065.3:c.626-56_626-52delinsTATCC , LRG_193t1:c.626-56_626-52delinsTATCC	NP_001056.1:n.626-56_626-52delinsTATCC
NM_001346091.1:c.302-56_302-52delinsTATCC	NP_001333020.1:n.302-56_302-52delinsTATCC
NM_001346092.1:c.167-56_167-52delinsTATCC	NP_001333021.1:n.167-56_167-52delinsTATCC
NR_144351.1:n.855-56_855-52delinsTATCC
NM_001065.4:c.626-56_626-52delinsTATCC MANE Select	NP_001056.1:n.626-56_626-52delinsTATCC
NM_001346091.2:c.302-56_302-52delinsTATCC	NP_001333020.1:n.302-56_302-52delinsTATCC
NM_001346092.2:c.167-56_167-52delinsTATCC	NP_001333021.1:n.167-56_167-52delinsTATCC
NR_144351.2:n.814-56_814-52delinsTATCC