Canonical Allele Identifier: CA383548079

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6440059G>T (hg19) ; chr12:g.6330893G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330893G>T , CM000674.2:g.6330893G>T	GRCh38
NC_000012.11:g.6440059G>T , CM000674.1:g.6440059G>T	GRCh37
NC_000012.10:g.6310320G>T	NCBI36
NG_007506.1:g.16203C>A , LRG_193:g.16203C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1686C>A
ENST00000437813.8:c.*46C>A	ENSP00000513672.1:n.*46C>A
ENST00000440083.7:c.804C>A	ENSP00000413224.3:p.Cys268Ter
ENST00000535038.2:n.767C>A
ENST00000535958.2:c.*412C>A	ENSP00000513673.1:n.*412C>A
ENST00000698337.1:n.434C>A
ENST00000698338.1:n.858C>A
ENST00000698339.1:c.*80C>A	ENSP00000513670.1:n.*80C>A
ENST00000698340.1:c.552-182C>A	ENSP00000513671.1:n.552-182C>A
ENST00000162749.7:c.585C>A MANE Select	ENSP00000162749.2:p.Cys195Ter
ENST00000162749.6:c.585C>A	ENSP00000162749.2:p.Cys195Ter
ENST00000534885.5:c.*62C>A	ENSP00000441803.1:n.*62C>A
ENST00000535038.1:n.255C>A
ENST00000536717.5:n.489C>A
ENST00000537842.5:n.189C>A
ENST00000539372.5:c.585C>A	ENSP00000442059.1:p.Cys195Ter
ENST00000540022.5:c.456C>A	ENSP00000438343.1:p.Cys152Ter
ENST00000543359.5:n.38-182C>A
ENST00000543995.5:c.*172C>A	ENSP00000442405.1:n.*172C>A
NM_001065.3:c.585C>A , LRG_193t1:c.585C>A	NP_001056.1:p.Cys195Ter
NM_001346091.1:c.261C>A	NP_001333020.1:p.Cys87Ter
NM_001346092.1:c.126C>A	NP_001333021.1:p.Cys42Ter
NR_144351.1:n.855-182C>A
NM_001065.4:c.585C>A MANE Select	NP_001056.1:p.Cys195Ter
NM_001346091.2:c.261C>A	NP_001333020.1:p.Cys87Ter
NM_001346092.2:c.126C>A	NP_001333021.1:p.Cys42Ter
NR_144351.2:n.814-182C>A