Canonical Allele Identifier: CA383545653

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6438982T>A (hg19) ; chr12:g.6329816T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6329816T>A , CM000674.2:g.6329816T>A	GRCh38
NC_000012.11:g.6438982T>A , CM000674.1:g.6438982T>A	GRCh37
NC_000012.10:g.6309243T>A	NCBI36
NG_007506.1:g.17280A>T , LRG_193:g.17280A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000366159.9:n.2120A>T
ENST00000437813.8:c.*480A>T	ENSP00000513672.1:n.*480A>T
ENST00000440083.7:c.1238A>T	ENSP00000413224.3:p.Lys413Met
ENST00000535958.2:c.*846A>T	ENSP00000513673.1:n.*846A>T
ENST00000698337.1:n.980A>T
ENST00000698338.1:n.1633A>T
ENST00000698339.1:c.*514A>T	ENSP00000513670.1:n.*514A>T
ENST00000698340.1:c.*258A>T	ENSP00000513671.1:n.*258A>T
ENST00000162749.7:c.1019A>T MANE Select	ENSP00000162749.2:p.Lys340Met
ENST00000162749.6:c.1019A>T	ENSP00000162749.2:p.Lys340Met
ENST00000534885.5:c.*496A>T	ENSP00000441803.1:n.*496A>T
ENST00000536717.5:n.923A>T
ENST00000540022.5:c.890A>T	ENSP00000438343.1:p.Lys297Met
ENST00000543359.5:n.431A>T
ENST00000543995.5:c.*606A>T	ENSP00000442405.1:n.*606A>T
NM_001065.3:c.1019A>T , LRG_193t1:c.1019A>T	NP_001056.1:p.Lys340Met
NM_001346091.1:c.695A>T	NP_001333020.1:p.Lys232Met
NM_001346092.1:c.560A>T	NP_001333021.1:p.Lys187Met
NR_144351.1:n.1248A>T
NM_001065.4:c.1019A>T MANE Select	NP_001056.1:p.Lys340Met
NM_001346091.2:c.695A>T	NP_001333020.1:p.Lys232Met
NM_001346092.2:c.560A>T	NP_001333021.1:p.Lys187Met
NR_144351.2:n.1207A>T