Canonical Allele Identifier: CA383548010

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6440037T>G (hg19) ; chr12:g.6330871T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330871T>G , CM000674.2:g.6330871T>G	GRCh38
NC_000012.11:g.6440037T>G , CM000674.1:g.6440037T>G	GRCh37
NC_000012.10:g.6310298T>G	NCBI36
NG_007506.1:g.16225A>C , LRG_193:g.16225A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1708A>C
ENST00000437813.8:c.*68A>C	ENSP00000513672.1:n.*68A>C
ENST00000440083.7:c.826A>C	ENSP00000413224.3:p.Lys276Gln
ENST00000535038.2:n.789A>C
ENST00000535958.2:c.*434A>C	ENSP00000513673.1:n.*434A>C
ENST00000698337.1:n.456A>C
ENST00000698338.1:n.880A>C
ENST00000698339.1:c.*102A>C	ENSP00000513670.1:n.*102A>C
ENST00000698340.1:c.552-160A>C	ENSP00000513671.1:n.552-160A>C
ENST00000162749.7:c.607A>C MANE Select	ENSP00000162749.2:p.Lys203Gln
ENST00000162749.6:c.607A>C	ENSP00000162749.2:p.Lys203Gln
ENST00000534885.5:c.*84A>C	ENSP00000441803.1:n.*84A>C
ENST00000535038.1:n.277A>C
ENST00000536717.5:n.511A>C
ENST00000537842.5:n.211A>C
ENST00000539372.5:c.607A>C	ENSP00000442059.1:p.Lys203Gln
ENST00000540022.5:c.478A>C	ENSP00000438343.1:p.Lys160Gln
ENST00000543359.5:n.38-160A>C
ENST00000543995.5:c.*194A>C	ENSP00000442405.1:n.*194A>C
NM_001065.3:c.607A>C , LRG_193t1:c.607A>C	NP_001056.1:p.Lys203Gln
NM_001346091.1:c.283A>C	NP_001333020.1:p.Lys95Gln
NM_001346092.1:c.148A>C	NP_001333021.1:p.Lys50Gln
NR_144351.1:n.855-160A>C
NM_001065.4:c.607A>C MANE Select	NP_001056.1:p.Lys203Gln
NM_001346091.2:c.283A>C	NP_001333020.1:p.Lys95Gln
NM_001346092.2:c.148A>C	NP_001333021.1:p.Lys50Gln
NR_144351.2:n.814-160A>C