Canonical Allele Identifier: CA478112892

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6440079G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330913G>A , CM000674.2:g.6330913G>A	GRCh38
NC_000012.11:g.6440079G>A , CM000674.1:g.6440079G>A	GRCh37
NC_000012.10:g.6310340G>A	NCBI36
NG_007506.1:g.16183C>T , LRG_193:g.16183C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1666C>T
ENST00000437813.8:c.*26C>T	ENSP00000513672.1:n.*26C>T
ENST00000440083.7:c.784C>T	ENSP00000413224.3:p.Leu262=
ENST00000535038.2:n.747C>T
ENST00000535958.2:c.*392C>T	ENSP00000513673.1:n.*392C>T
ENST00000698337.1:n.414C>T
ENST00000698338.1:n.838C>T
ENST00000698339.1:c.*60C>T	ENSP00000513670.1:n.*60C>T
ENST00000698340.1:c.552-202C>T	ENSP00000513671.1:n.552-202C>T
ENST00000162749.7:c.565C>T MANE Select	ENSP00000162749.2:p.Leu189=
ENST00000162749.6:c.565C>T	ENSP00000162749.2:p.Leu189=
ENST00000534885.5:c.*42C>T	ENSP00000441803.1:n.*42C>T
ENST00000535038.1:n.235C>T
ENST00000536717.5:n.469C>T
ENST00000537842.5:n.169C>T
ENST00000539372.5:c.565C>T	ENSP00000442059.1:p.Leu189=
ENST00000540022.5:c.436C>T	ENSP00000438343.1:p.Leu146=
ENST00000543359.5:n.38-202C>T
ENST00000543995.5:c.*152C>T	ENSP00000442405.1:n.*152C>T
NM_001065.3:c.565C>T , LRG_193t1:c.565C>T	NP_001056.1:p.Leu189=
NM_001346091.1:c.241C>T	NP_001333020.1:p.Leu81=
NM_001346092.1:c.106C>T	NP_001333021.1:p.Leu36=
NR_144351.1:n.855-202C>T
NM_001065.4:c.565C>T MANE Select	NP_001056.1:p.Leu189=
NM_001346091.2:c.241C>T	NP_001333020.1:p.Leu81=
NM_001346092.2:c.106C>T	NP_001333021.1:p.Leu36=
NR_144351.2:n.814-202C>T