Canonical Allele Identifier: CA383545639

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6438976T>A (hg19) ; chr12:g.6329810T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6329810T>A , CM000674.2:g.6329810T>A	GRCh38
NC_000012.11:g.6438976T>A , CM000674.1:g.6438976T>A	GRCh37
NC_000012.10:g.6309237T>A	NCBI36
NG_007506.1:g.17286A>T , LRG_193:g.17286A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000366159.9:n.2126A>T
ENST00000437813.8:c.*486A>T	ENSP00000513672.1:n.*486A>T
ENST00000440083.7:c.1244A>T	ENSP00000413224.3:p.Glu415Val
ENST00000535958.2:c.*852A>T	ENSP00000513673.1:n.*852A>T
ENST00000698337.1:n.986A>T
ENST00000698338.1:n.1639A>T
ENST00000698339.1:c.*520A>T	ENSP00000513670.1:n.*520A>T
ENST00000698340.1:c.*264A>T	ENSP00000513671.1:n.*264A>T
ENST00000162749.7:c.1025A>T MANE Select	ENSP00000162749.2:p.Glu342Val
ENST00000162749.6:c.1025A>T	ENSP00000162749.2:p.Glu342Val
ENST00000534885.5:c.*502A>T	ENSP00000441803.1:n.*502A>T
ENST00000536717.5:n.929A>T
ENST00000540022.5:c.896A>T	ENSP00000438343.1:p.Glu299Val
ENST00000543359.5:n.437A>T
ENST00000543995.5:c.*612A>T	ENSP00000442405.1:n.*612A>T
NM_001065.3:c.1025A>T , LRG_193t1:c.1025A>T	NP_001056.1:p.Glu342Val
NM_001346091.1:c.701A>T	NP_001333020.1:p.Glu234Val
NM_001346092.1:c.566A>T	NP_001333021.1:p.Glu189Val
NR_144351.1:n.1254A>T
NM_001065.4:c.1025A>T MANE Select	NP_001056.1:p.Glu342Val
NM_001346091.2:c.701A>T	NP_001333020.1:p.Glu234Val
NM_001346092.2:c.566A>T	NP_001333021.1:p.Glu189Val
NR_144351.2:n.1213A>T