Canonical Allele Identifier: CA232331230

Gene: TNFRSF1A

Linked Data

• dbSNP Id: rs528802948
• gnomAD v2: 12-6443676-AT-A
• gnomAD v3: 12-6334510-AT-A
• gnomAD v4: 12-6334510-AT-A
• MyVariant Identifiers: chr12:g.6443678del (hg19) ; chr12:g.6443677del (hg19) ; chr12:g.6334512del (hg38) ; chr12:g.6334511del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6334523del , CM000674.2:g.6334523del	GRCh38
NC_000012.11:g.6443689del , CM000674.1:g.6443689del	GRCh37
NC_000012.10:g.6313950del	NCBI36
NG_007506.1:g.12585del , LRG_193:g.12585del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.74-267del
ENST00000437813.8:c.40-267del	ENSP00000513672.1:n.40-267del
ENST00000440083.7:c.40-267del	ENSP00000413224.3:n.40-267del
ENST00000535958.2:c.40-267del	ENSP00000513673.1:n.40-267del
ENST00000698339.1:c.40-267del	ENSP00000513670.1:n.40-267del
ENST00000698340.1:c.40-267del	ENSP00000513671.1:n.40-267del
ENST00000162749.7:c.40-267del MANE Select	ENSP00000162749.2:n.40-267del
ENST00000162749.6:c.40-267del	ENSP00000162749.2:n.40-267del
ENST00000366159.8:c.40-267del	ENSP00000380389.3:n.40-267del
ENST00000440083.6:c.40-267del	ENSP00000413224.2:n.40-267del
ENST00000534885.5:c.40-646del	ENSP00000441803.1:n.40-646del
ENST00000535958.1:n.261-267del
ENST00000536194.1:c.40-267del	ENSP00000442919.1:n.40-267del
ENST00000538363.1:n.230-267del
ENST00000539372.5:c.40-267del	ENSP00000442059.1:n.40-267del
ENST00000540022.5:c.40-267del	ENSP00000438343.1:n.40-267del
ENST00000543048.5:c.40-267del	ENSP00000439981.1:n.40-267del
ENST00000543995.5:c.40-267del	ENSP00000442405.1:n.40-267del
NM_001065.3:c.40-267del , LRG_193t1:c.40-267del	NP_001056.1:n.40-267del
NM_001346091.1:c.-131-646del	NP_001333020.1:n.-131-646del
NM_001346092.1:c.-538-267del	NP_001333021.1:n.-538-267del
NR_144351.1:n.343-267del
NM_001065.4:c.40-267del MANE Select	NP_001056.1:n.40-267del
NM_001346091.2:c.-131-646del	NP_001333020.1:n.-131-646del
NM_001346092.2:c.-538-267del	NP_001333021.1:n.-538-267del
NR_144351.2:n.302-267del