Canonical Allele Identifier: CA383548018

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6440042T>A (hg19) ; chr12:g.6330876T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330876T>A , CM000674.2:g.6330876T>A	GRCh38
NC_000012.11:g.6440042T>A , CM000674.1:g.6440042T>A	GRCh37
NC_000012.10:g.6310303T>A	NCBI36
NG_007506.1:g.16220A>T , LRG_193:g.16220A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1703A>T
ENST00000437813.8:c.*63A>T	ENSP00000513672.1:n.*63A>T
ENST00000440083.7:c.821A>T	ENSP00000413224.3:p.Asn274Ile
ENST00000535038.2:n.784A>T
ENST00000535958.2:c.*429A>T	ENSP00000513673.1:n.*429A>T
ENST00000698337.1:n.451A>T
ENST00000698338.1:n.875A>T
ENST00000698339.1:c.*97A>T	ENSP00000513670.1:n.*97A>T
ENST00000698340.1:c.552-165A>T	ENSP00000513671.1:n.552-165A>T
ENST00000162749.7:c.602A>T MANE Select	ENSP00000162749.2:p.Asn201Ile
ENST00000162749.6:c.602A>T	ENSP00000162749.2:p.Asn201Ile
ENST00000534885.5:c.*79A>T	ENSP00000441803.1:n.*79A>T
ENST00000535038.1:n.272A>T
ENST00000536717.5:n.506A>T
ENST00000537842.5:n.206A>T
ENST00000539372.5:c.602A>T	ENSP00000442059.1:p.Asn201Ile
ENST00000540022.5:c.473A>T	ENSP00000438343.1:p.Asn158Ile
ENST00000543359.5:n.38-165A>T
ENST00000543995.5:c.*189A>T	ENSP00000442405.1:n.*189A>T
NM_001065.3:c.602A>T , LRG_193t1:c.602A>T	NP_001056.1:p.Asn201Ile
NM_001346091.1:c.278A>T	NP_001333020.1:p.Asn93Ile
NM_001346092.1:c.143A>T	NP_001333021.1:p.Asn48Ile
NR_144351.1:n.855-165A>T
NM_001065.4:c.602A>T MANE Select	NP_001056.1:p.Asn201Ile
NM_001346091.2:c.278A>T	NP_001333020.1:p.Asn93Ile
NM_001346092.2:c.143A>T	NP_001333021.1:p.Asn48Ile
NR_144351.2:n.814-165A>T