Canonical Allele Identifier: CA383549071

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6442272A>T (hg19) ; chr12:g.6333106A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6333106A>T , CM000674.2:g.6333106A>T	GRCh38
NC_000012.11:g.6442272A>T , CM000674.1:g.6442272A>T	GRCh37
NC_000012.10:g.6312533A>T	NCBI36
NG_007506.1:g.13990T>A , LRG_193:g.13990T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.548T>A
ENST00000437813.8:c.514T>A	ENSP00000513672.1:p.Phe172Ile
ENST00000440083.7:c.733T>A	ENSP00000413224.3:p.Phe245Ile
ENST00000535958.2:c.*341T>A	ENSP00000513673.1:n.*341T>A
ENST00000698339.1:c.514T>A	ENSP00000513670.1:p.Phe172Ile
ENST00000698340.1:c.514T>A	ENSP00000513671.1:p.Phe172Ile
ENST00000162749.7:c.514T>A MANE Select	ENSP00000162749.2:p.Phe172Ile
ENST00000162749.6:c.514T>A	ENSP00000162749.2:p.Phe172Ile
ENST00000366159.8:c.514T>A	ENSP00000380389.3:p.Phe172Ile
ENST00000437813.7:n.475T>A
ENST00000440083.6:c.733T>A	ENSP00000413224.2:p.Phe245Ile
ENST00000534885.5:c.360T>A	ENSP00000441803.1:p.Val120=
ENST00000537842.5:n.118T>A
ENST00000539372.5:c.514T>A	ENSP00000442059.1:p.Phe172Ile
ENST00000540022.5:c.385T>A	ENSP00000438343.1:p.Phe129Ile
ENST00000543048.5:c.*125T>A	ENSP00000439981.1:n.*125T>A
ENST00000543995.5:c.*101T>A	ENSP00000442405.1:n.*101T>A
NM_001065.3:c.514T>A , LRG_193t1:c.514T>A	NP_001056.1:p.Phe172Ile
NM_001346091.1:c.190T>A	NP_001333020.1:p.Phe64Ile
NM_001346092.1:c.-64T>A	NP_001333021.1:n.-64T>A
NR_144351.1:n.817T>A
NM_001065.4:c.514T>A MANE Select	NP_001056.1:p.Phe172Ile
NM_001346091.2:c.190T>A	NP_001333020.1:p.Phe64Ile
NM_001346092.2:c.-64T>A	NP_001333021.1:n.-64T>A
NR_144351.2:n.776T>A