Canonical Allele Identifier: CA383550226

Gene: TNFRSF1A

Linked Data

• gnomAD v3: 12-6333480-T-A
• gnomAD v4: 12-6333480-T-A
• MyVariant Identifiers: chr12:g.6442646T>A (hg19) ; chr12:g.6333480T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6333480T>A , CM000674.2:g.6333480T>A	GRCh38
NC_000012.11:g.6442646T>A , CM000674.1:g.6442646T>A	GRCh37
NC_000012.10:g.6312907T>A	NCBI36
NG_007506.1:g.13616A>T , LRG_193:g.13616A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.393A>T
ENST00000437813.8:c.359A>T	ENSP00000513672.1:p.Asp120Val
ENST00000440083.7:c.359A>T	ENSP00000413224.3:p.Asp120Val
ENST00000535958.2:c.*186A>T	ENSP00000513673.1:n.*186A>T
ENST00000698339.1:c.359A>T	ENSP00000513670.1:p.Asp120Val
ENST00000698340.1:c.359A>T	ENSP00000513671.1:p.Asp120Val
ENST00000162749.7:c.359A>T MANE Select	ENSP00000162749.2:p.Asp120Val
ENST00000162749.6:c.359A>T	ENSP00000162749.2:p.Asp120Val
ENST00000366159.8:c.359A>T	ENSP00000380389.3:p.Asp120Val
ENST00000437813.7:n.320A>T
ENST00000440083.6:c.359A>T	ENSP00000413224.2:p.Asp120Val
ENST00000534885.5:c.205A>T	ENSP00000441803.1:p.Thr69Ser
ENST00000536194.1:c.332A>T	ENSP00000442919.1:p.Asp111Val
ENST00000539372.5:c.359A>T	ENSP00000442059.1:p.Asp120Val
ENST00000540022.5:c.230A>T	ENSP00000438343.1:p.Asp77Val
ENST00000543048.5:c.215-29A>T	ENSP00000439981.1:n.215-29A>T
ENST00000543995.5:c.194-29A>T	ENSP00000442405.1:n.194-29A>T
NM_001065.3:c.359A>T , LRG_193t1:c.359A>T	NP_001056.1:p.Asp120Val
NM_001346091.1:c.35A>T	NP_001333020.1:p.Asp12Val
NM_001346092.1:c.-219A>T	NP_001333021.1:n.-219A>T
NR_144351.1:n.662A>T
NM_001065.4:c.359A>T MANE Select	NP_001056.1:p.Asp120Val
NM_001346091.2:c.35A>T	NP_001333020.1:p.Asp12Val
NM_001346092.2:c.-219A>T	NP_001333021.1:n.-219A>T
NR_144351.2:n.621A>T