Canonical Allele Identifier: CA383549146

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6442305T>A (hg19) ; chr12:g.6333139T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6333139T>A , CM000674.2:g.6333139T>A	GRCh38
NC_000012.11:g.6442305T>A , CM000674.1:g.6442305T>A	GRCh37
NC_000012.10:g.6312566T>A	NCBI36
NG_007506.1:g.13957A>T , LRG_193:g.13957A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.515A>T
ENST00000437813.8:c.481A>T	ENSP00000513672.1:p.Lys161Ter
ENST00000440083.7:c.700A>T	ENSP00000413224.3:p.Lys234Ter
ENST00000535958.2:c.*308A>T	ENSP00000513673.1:n.*308A>T
ENST00000698339.1:c.481A>T	ENSP00000513670.1:p.Lys161Ter
ENST00000698340.1:c.481A>T	ENSP00000513671.1:p.Lys161Ter
ENST00000162749.7:c.481A>T MANE Select	ENSP00000162749.2:p.Lys161Ter
ENST00000162749.6:c.481A>T	ENSP00000162749.2:p.Lys161Ter
ENST00000366159.8:c.481A>T	ENSP00000380389.3:p.Lys161Ter
ENST00000437813.7:n.442A>T
ENST00000440083.6:c.700A>T	ENSP00000413224.2:p.Lys234Ter
ENST00000534885.5:c.327A>T	ENSP00000441803.1:p.Arg109Ser
ENST00000537842.5:n.85A>T
ENST00000539372.5:c.481A>T	ENSP00000442059.1:p.Lys161Ter
ENST00000540022.5:c.352A>T	ENSP00000438343.1:p.Lys118Ter
ENST00000543048.5:c.*92A>T	ENSP00000439981.1:n.*92A>T
ENST00000543995.5:c.*68A>T	ENSP00000442405.1:n.*68A>T
NM_001065.3:c.481A>T , LRG_193t1:c.481A>T	NP_001056.1:p.Lys161Ter
NM_001346091.1:c.157A>T	NP_001333020.1:p.Lys53Ter
NM_001346092.1:c.-97A>T	NP_001333021.1:n.-97A>T
NR_144351.1:n.784A>T
NM_001065.4:c.481A>T MANE Select	NP_001056.1:p.Lys161Ter
NM_001346091.2:c.157A>T	NP_001333020.1:p.Lys53Ter
NM_001346092.2:c.-97A>T	NP_001333021.1:n.-97A>T
NR_144351.2:n.743A>T