Canonical Allele Identifier: CA603483442

Gene: TNFRSF1A

Linked Data

• dbSNP Id: rs1565468272
• gnomAD v2: 12-6443057-CT-C
• gnomAD v4: 12-6333891-CT-C
• MyVariant Identifiers: chr12:g.6443058del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6333892del , CM000674.2:g.6333892del	GRCh38
NC_000012.11:g.6443058del , CM000674.1:g.6443058del	GRCh37
NC_000012.10:g.6313319del	NCBI36
NG_007506.1:g.13204del , LRG_193:g.13204del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.228-27del
ENST00000437813.8:c.194-27del	ENSP00000513672.1:n.194-27del
ENST00000440083.7:c.194-27del	ENSP00000413224.3:n.194-27del
ENST00000535958.2:c.194-2del	ENSP00000513673.1:n.194-2del
ENST00000698339.1:c.194-27del	ENSP00000513670.1:n.194-27del
ENST00000698340.1:c.194-27del	ENSP00000513671.1:n.194-27del
ENST00000162749.7:c.194-27del MANE Select	ENSP00000162749.2:n.194-27del
ENST00000162749.6:c.194-27del	ENSP00000162749.2:n.194-27del
ENST00000366159.8:c.194-27del	ENSP00000380389.3:n.194-27del
ENST00000437813.7:n.155-27del
ENST00000440083.6:c.194-27del	ENSP00000413224.2:n.194-27del
ENST00000534885.5:c.40-27del	ENSP00000441803.1:n.40-27del
ENST00000535958.1:n.415-2del
ENST00000536194.1:c.194-54del	ENSP00000442919.1:n.194-54del
ENST00000539372.5:c.194-27del	ENSP00000442059.1:n.194-27del
ENST00000540022.5:c.193+199del	ENSP00000438343.1:n.193+199del
ENST00000543048.5:c.194-27del	ENSP00000439981.1:n.194-27del
ENST00000543995.5:c.193+199del	ENSP00000442405.1:n.193+199del
NM_001065.3:c.194-27del , LRG_193t1:c.194-27del	NP_001056.1:n.194-27del
NM_001346091.1:c.-131-27del	NP_001333020.1:n.-131-27del
NM_001346092.1:c.-384-27del	NP_001333021.1:n.-384-27del
NR_144351.1:n.497-27del
NM_001065.4:c.194-27del MANE Select	NP_001056.1:n.194-27del
NM_001346091.2:c.-131-27del	NP_001333020.1:n.-131-27del
NM_001346092.2:c.-384-27del	NP_001333021.1:n.-384-27del
NR_144351.2:n.456-27del