Canonical Allele Identifier: CA383547665

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6439820A>T (hg19) ; chr12:g.6330654A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330654A>T , CM000674.2:g.6330654A>T	GRCh38
NC_000012.11:g.6439820A>T , CM000674.1:g.6439820A>T	GRCh37
NC_000012.10:g.6310081A>T	NCBI36
NG_007506.1:g.16442T>A , LRG_193:g.16442T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1784T>A
ENST00000437813.8:c.*144T>A	ENSP00000513672.1:n.*144T>A
ENST00000440083.7:c.902T>A	ENSP00000413224.3:p.Leu301His
ENST00000535038.2:n.865T>A
ENST00000535958.2:c.*510T>A	ENSP00000513673.1:n.*510T>A
ENST00000698337.1:n.673T>A
ENST00000698338.1:n.1097T>A
ENST00000698339.1:c.*178T>A	ENSP00000513670.1:n.*178T>A
ENST00000698340.1:c.609T>A	ENSP00000513671.1:p.Pro203=
ENST00000162749.7:c.683T>A MANE Select	ENSP00000162749.2:p.Leu228His
ENST00000162749.6:c.683T>A	ENSP00000162749.2:p.Leu228His
ENST00000534885.5:c.*160T>A	ENSP00000441803.1:n.*160T>A
ENST00000535038.1:n.494T>A
ENST00000536717.5:n.587T>A
ENST00000537842.5:n.287T>A
ENST00000539372.5:c.683T>A	ENSP00000442059.1:p.Leu228His
ENST00000540022.5:c.554T>A	ENSP00000438343.1:p.Leu185His
ENST00000543359.5:n.95T>A
ENST00000543995.5:c.*270T>A	ENSP00000442405.1:n.*270T>A
NM_001065.3:c.683T>A , LRG_193t1:c.683T>A	NP_001056.1:p.Leu228His
NM_001346091.1:c.359T>A	NP_001333020.1:p.Leu120His
NM_001346092.1:c.224T>A	NP_001333021.1:p.Leu75His
NR_144351.1:n.912T>A
NM_001065.4:c.683T>A MANE Select	NP_001056.1:p.Leu228His
NM_001346091.2:c.359T>A	NP_001333020.1:p.Leu120His
NM_001346092.2:c.224T>A	NP_001333021.1:p.Leu75His
NR_144351.2:n.871T>A