Canonical Allele Identifier: CA478112695

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6440023G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330857G>A , CM000674.2:g.6330857G>A	GRCh38
NC_000012.11:g.6440023G>A , CM000674.1:g.6440023G>A	GRCh37
NC_000012.10:g.6310284G>A	NCBI36
NG_007506.1:g.16239C>T , LRG_193:g.16239C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1722C>T
ENST00000437813.8:c.*82C>T	ENSP00000513672.1:n.*82C>T
ENST00000440083.7:c.840C>T	ENSP00000413224.3:p.Asp280=
ENST00000535038.2:n.803C>T
ENST00000535958.2:c.*448C>T	ENSP00000513673.1:n.*448C>T
ENST00000698337.1:n.470C>T
ENST00000698338.1:n.894C>T
ENST00000698339.1:c.*116C>T	ENSP00000513670.1:n.*116C>T
ENST00000698340.1:c.552-146C>T	ENSP00000513671.1:n.552-146C>T
ENST00000162749.7:c.621C>T MANE Select	ENSP00000162749.2:p.Asp207=
ENST00000162749.6:c.621C>T	ENSP00000162749.2:p.Asp207=
ENST00000534885.5:c.*98C>T	ENSP00000441803.1:n.*98C>T
ENST00000535038.1:n.291C>T
ENST00000536717.5:n.525C>T
ENST00000537842.5:n.225C>T
ENST00000539372.5:c.621C>T	ENSP00000442059.1:p.Asp207=
ENST00000540022.5:c.492C>T	ENSP00000438343.1:p.Asp164=
ENST00000543359.5:n.38-146C>T
ENST00000543995.5:c.*208C>T	ENSP00000442405.1:n.*208C>T
NM_001065.3:c.621C>T , LRG_193t1:c.621C>T	NP_001056.1:p.Asp207=
NM_001346091.1:c.297C>T	NP_001333020.1:p.Asp99=
NM_001346092.1:c.162C>T	NP_001333021.1:p.Asp54=
NR_144351.1:n.855-146C>T
NM_001065.4:c.621C>T MANE Select	NP_001056.1:p.Asp207=
NM_001346091.2:c.297C>T	NP_001333020.1:p.Asp99=
NM_001346092.2:c.162C>T	NP_001333021.1:p.Asp54=
NR_144351.2:n.814-146C>T