Canonical Allele Identifier: CA383548007

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6440036T>G (hg19) ; chr12:g.6330870T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330870T>G , CM000674.2:g.6330870T>G	GRCh38
NC_000012.11:g.6440036T>G , CM000674.1:g.6440036T>G	GRCh37
NC_000012.10:g.6310297T>G	NCBI36
NG_007506.1:g.16226A>C , LRG_193:g.16226A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1709A>C
ENST00000437813.8:c.*69A>C	ENSP00000513672.1:n.*69A>C
ENST00000440083.7:c.827A>C	ENSP00000413224.3:p.Lys276Thr
ENST00000535038.2:n.790A>C
ENST00000535958.2:c.*435A>C	ENSP00000513673.1:n.*435A>C
ENST00000698337.1:n.457A>C
ENST00000698338.1:n.881A>C
ENST00000698339.1:c.*103A>C	ENSP00000513670.1:n.*103A>C
ENST00000698340.1:c.552-159A>C	ENSP00000513671.1:n.552-159A>C
ENST00000162749.7:c.608A>C MANE Select	ENSP00000162749.2:p.Lys203Thr
ENST00000162749.6:c.608A>C	ENSP00000162749.2:p.Lys203Thr
ENST00000534885.5:c.*85A>C	ENSP00000441803.1:n.*85A>C
ENST00000535038.1:n.278A>C
ENST00000536717.5:n.512A>C
ENST00000537842.5:n.212A>C
ENST00000539372.5:c.608A>C	ENSP00000442059.1:p.Lys203Thr
ENST00000540022.5:c.479A>C	ENSP00000438343.1:p.Lys160Thr
ENST00000543359.5:n.38-159A>C
ENST00000543995.5:c.*195A>C	ENSP00000442405.1:n.*195A>C
NM_001065.3:c.608A>C , LRG_193t1:c.608A>C	NP_001056.1:p.Lys203Thr
NM_001346091.1:c.284A>C	NP_001333020.1:p.Lys95Thr
NM_001346092.1:c.149A>C	NP_001333021.1:p.Lys50Thr
NR_144351.1:n.855-159A>C
NM_001065.4:c.608A>C MANE Select	NP_001056.1:p.Lys203Thr
NM_001346091.2:c.284A>C	NP_001333020.1:p.Lys95Thr
NM_001346092.2:c.149A>C	NP_001333021.1:p.Lys50Thr
NR_144351.2:n.814-159A>C