Canonical Allele Identifier: CA383550028

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6442589T>A (hg19) ; chr12:g.6333423T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6333423T>A , CM000674.2:g.6333423T>A	GRCh38
NC_000012.11:g.6442589T>A , CM000674.1:g.6442589T>A	GRCh37
NC_000012.10:g.6312850T>A	NCBI36
NG_007506.1:g.13673A>T , LRG_193:g.13673A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.450A>T
ENST00000437813.8:c.416A>T	ENSP00000513672.1:p.Asn139Ile
ENST00000440083.7:c.416A>T	ENSP00000413224.3:p.Asn139Ile
ENST00000535958.2:c.*243A>T	ENSP00000513673.1:n.*243A>T
ENST00000698339.1:c.416A>T	ENSP00000513670.1:p.Asn139Ile
ENST00000698340.1:c.416A>T	ENSP00000513671.1:p.Asn139Ile
ENST00000162749.7:c.416A>T MANE Select	ENSP00000162749.2:p.Asn139Ile
ENST00000162749.6:c.416A>T	ENSP00000162749.2:p.Asn139Ile
ENST00000366159.8:c.416A>T	ENSP00000380389.3:p.Asn139Ile
ENST00000437813.7:n.377A>T
ENST00000440083.6:c.416A>T	ENSP00000413224.2:p.Asn139Ile
ENST00000534885.5:c.262A>T	ENSP00000441803.1:p.Thr88Ser
ENST00000537842.5:n.20A>T
ENST00000539372.5:c.416A>T	ENSP00000442059.1:p.Asn139Ile
ENST00000540022.5:c.287A>T	ENSP00000438343.1:p.Asn96Ile
ENST00000543048.5:c.*27A>T	ENSP00000439981.1:n.*27A>T
ENST00000543995.5:c.*3A>T	ENSP00000442405.1:n.*3A>T
NM_001065.3:c.416A>T , LRG_193t1:c.416A>T	NP_001056.1:p.Asn139Ile
NM_001346091.1:c.92A>T	NP_001333020.1:p.Asn31Ile
NM_001346092.1:c.-162A>T	NP_001333021.1:n.-162A>T
NR_144351.1:n.719A>T
NM_001065.4:c.416A>T MANE Select	NP_001056.1:p.Asn139Ile
NM_001346091.2:c.92A>T	NP_001333020.1:p.Asn31Ile
NM_001346092.2:c.-162A>T	NP_001333021.1:n.-162A>T
NR_144351.2:n.678A>T