Canonical Allele Identifier: CA2617251024

Gene: TNFRSF1A

Linked Data

• gnomAD v4: 12-6330844-T-TCTC

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330848_6330850dup , CM000674.2:g.6330848_6330850dup	GRCh38
NC_000012.11:g.6440014_6440016dup , CM000674.1:g.6440014_6440016dup	GRCh37
NC_000012.10:g.6310275_6310277dup	NCBI36
NG_007506.1:g.16249_16251dup , LRG_193:g.16249_16251dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1726+6_1726+8dup
ENST00000437813.8:c.*86+6_*86+8dup	ENSP00000513672.1:n.*86+6_*86+8dup
ENST00000440083.7:c.844+6_844+8dup	ENSP00000413224.3:n.844+6_844+8dup
ENST00000535038.2:n.807+6_807+8dup
ENST00000535958.2:c.*452+6_*452+8dup	ENSP00000513673.1:n.*452+6_*452+8dup
ENST00000698337.1:n.480_482dup
ENST00000698338.1:n.904_906dup
ENST00000698339.1:c.*120+6_*120+8dup	ENSP00000513670.1:n.*120+6_*120+8dup
ENST00000698340.1:c.552-136_552-134dup	ENSP00000513671.1:n.552-136_552-134dup
ENST00000162749.7:c.625+6_625+8dup MANE Select	ENSP00000162749.2:n.625+6_625+8dup
ENST00000162749.6:c.625+6_625+8dup	ENSP00000162749.2:n.625+6_625+8dup
ENST00000534885.5:c.*102+6_*102+8dup	ENSP00000441803.1:n.*102+6_*102+8dup
ENST00000535038.1:n.301_303dup
ENST00000536717.5:n.529+6_529+8dup
ENST00000537842.5:n.229+6_229+8dup
ENST00000539372.5:c.625+6_625+8dup	ENSP00000442059.1:n.625+6_625+8dup
ENST00000540022.5:c.496+6_496+8dup	ENSP00000438343.1:n.496+6_496+8dup
ENST00000543359.5:n.38-136_38-134dup
ENST00000543995.5:c.*212+6_*212+8dup	ENSP00000442405.1:n.*212+6_*212+8dup
NM_001065.3:c.625+6_625+8dup , LRG_193t1:c.625+6_625+8dup	NP_001056.1:n.625+6_625+8dup
NM_001346091.1:c.301+6_301+8dup	NP_001333020.1:n.301+6_301+8dup
NM_001346092.1:c.166+6_166+8dup	NP_001333021.1:n.166+6_166+8dup
NR_144351.1:n.855-136_855-134dup
NM_001065.4:c.625+6_625+8dup MANE Select	NP_001056.1:n.625+6_625+8dup
NM_001346091.2:c.301+6_301+8dup	NP_001333020.1:n.301+6_301+8dup
NM_001346092.2:c.166+6_166+8dup	NP_001333021.1:n.166+6_166+8dup
NR_144351.2:n.814-136_814-134dup