Canonical Allele Identifier: CA603483603

Gene: TNFRSF1A

Linked Data

• dbSNP Id: rs1223554357
• gnomAD v2: 12-6439986-G-T
• gnomAD v4: 12-6330820-G-T
• MyVariant Identifiers: chr12:g.6439986G>T (hg19) ; chr12:g.6330820G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330820G>T , CM000674.2:g.6330820G>T	GRCh38
NC_000012.11:g.6439986G>T , CM000674.1:g.6439986G>T	GRCh37
NC_000012.10:g.6310247G>T	NCBI36
NG_007506.1:g.16276C>A , LRG_193:g.16276C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1726+33C>A
ENST00000437813.8:c.*86+33C>A	ENSP00000513672.1:n.*86+33C>A
ENST00000440083.7:c.844+33C>A	ENSP00000413224.3:n.844+33C>A
ENST00000535038.2:n.807+33C>A
ENST00000535958.2:c.*452+33C>A	ENSP00000513673.1:n.*452+33C>A
ENST00000698337.1:n.507C>A
ENST00000698338.1:n.931C>A
ENST00000698339.1:c.*120+33C>A	ENSP00000513670.1:n.*120+33C>A
ENST00000698340.1:c.552-109C>A	ENSP00000513671.1:n.552-109C>A
ENST00000162749.7:c.625+33C>A MANE Select	ENSP00000162749.2:n.625+33C>A
ENST00000162749.6:c.625+33C>A	ENSP00000162749.2:n.625+33C>A
ENST00000534885.5:c.*102+33C>A	ENSP00000441803.1:n.*102+33C>A
ENST00000535038.1:n.328C>A
ENST00000536717.5:n.529+33C>A
ENST00000537842.5:n.229+33C>A
ENST00000539372.5:c.625+33C>A	ENSP00000442059.1:n.625+33C>A
ENST00000540022.5:c.496+33C>A	ENSP00000438343.1:n.496+33C>A
ENST00000543359.5:n.38-109C>A
ENST00000543995.5:c.*212+33C>A	ENSP00000442405.1:n.*212+33C>A
NM_001065.3:c.625+33C>A , LRG_193t1:c.625+33C>A	NP_001056.1:n.625+33C>A
NM_001346091.1:c.301+33C>A	NP_001333020.1:n.301+33C>A
NM_001346092.1:c.166+33C>A	NP_001333021.1:n.166+33C>A
NR_144351.1:n.855-109C>A
NM_001065.4:c.625+33C>A MANE Select	NP_001056.1:n.625+33C>A
NM_001346091.2:c.301+33C>A	NP_001333020.1:n.301+33C>A
NM_001346092.2:c.166+33C>A	NP_001333021.1:n.166+33C>A
NR_144351.2:n.814-109C>A