Canonical Allele Identifier: CA383547743

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6439841C>A (hg19) ; chr12:g.6330675C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330675C>A , CM000674.2:g.6330675C>A	GRCh38
NC_000012.11:g.6439841C>A , CM000674.1:g.6439841C>A	GRCh37
NC_000012.10:g.6310102C>A	NCBI36
NG_007506.1:g.16421G>T , LRG_193:g.16421G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1763G>T
ENST00000437813.8:c.*123G>T	ENSP00000513672.1:n.*123G>T
ENST00000440083.7:c.881G>T	ENSP00000413224.3:p.Gly294Val
ENST00000535038.2:n.844G>T
ENST00000535958.2:c.*489G>T	ENSP00000513673.1:n.*489G>T
ENST00000698337.1:n.652G>T
ENST00000698338.1:n.1076G>T
ENST00000698339.1:c.*157G>T	ENSP00000513670.1:n.*157G>T
ENST00000698340.1:c.588G>T	ENSP00000513671.1:p.Trp196Cys
ENST00000162749.7:c.662G>T MANE Select	ENSP00000162749.2:p.Gly221Val
ENST00000162749.6:c.662G>T	ENSP00000162749.2:p.Gly221Val
ENST00000534885.5:c.*139G>T	ENSP00000441803.1:n.*139G>T
ENST00000535038.1:n.473G>T
ENST00000536717.5:n.566G>T
ENST00000537842.5:n.266G>T
ENST00000539372.5:c.662G>T	ENSP00000442059.1:p.Gly221Val
ENST00000540022.5:c.533G>T	ENSP00000438343.1:p.Gly178Val
ENST00000543359.5:n.74G>T
ENST00000543995.5:c.*249G>T	ENSP00000442405.1:n.*249G>T
NM_001065.3:c.662G>T , LRG_193t1:c.662G>T	NP_001056.1:p.Gly221Val
NM_001346091.1:c.338G>T	NP_001333020.1:p.Gly113Val
NM_001346092.1:c.203G>T	NP_001333021.1:p.Gly68Val
NR_144351.1:n.891G>T
NM_001065.4:c.662G>T MANE Select	NP_001056.1:p.Gly221Val
NM_001346091.2:c.338G>T	NP_001333020.1:p.Gly113Val
NM_001346092.2:c.203G>T	NP_001333021.1:p.Gly68Val
NR_144351.2:n.850G>T