Canonical Allele Identifier: CA383547956

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6440024T>A (hg19) ; chr12:g.6330858T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330858T>A , CM000674.2:g.6330858T>A	GRCh38
NC_000012.11:g.6440024T>A , CM000674.1:g.6440024T>A	GRCh37
NC_000012.10:g.6310285T>A	NCBI36
NG_007506.1:g.16238A>T , LRG_193:g.16238A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1721A>T
ENST00000437813.8:c.*81A>T	ENSP00000513672.1:n.*81A>T
ENST00000440083.7:c.839A>T	ENSP00000413224.3:p.Asp280Val
ENST00000535038.2:n.802A>T
ENST00000535958.2:c.*447A>T	ENSP00000513673.1:n.*447A>T
ENST00000698337.1:n.469A>T
ENST00000698338.1:n.893A>T
ENST00000698339.1:c.*115A>T	ENSP00000513670.1:n.*115A>T
ENST00000698340.1:c.552-147A>T	ENSP00000513671.1:n.552-147A>T
ENST00000162749.7:c.620A>T MANE Select	ENSP00000162749.2:p.Asp207Val
ENST00000162749.6:c.620A>T	ENSP00000162749.2:p.Asp207Val
ENST00000534885.5:c.*97A>T	ENSP00000441803.1:n.*97A>T
ENST00000535038.1:n.290A>T
ENST00000536717.5:n.524A>T
ENST00000537842.5:n.224A>T
ENST00000539372.5:c.620A>T	ENSP00000442059.1:p.Asp207Val
ENST00000540022.5:c.491A>T	ENSP00000438343.1:p.Asp164Val
ENST00000543359.5:n.38-147A>T
ENST00000543995.5:c.*207A>T	ENSP00000442405.1:n.*207A>T
NM_001065.3:c.620A>T , LRG_193t1:c.620A>T	NP_001056.1:p.Asp207Val
NM_001346091.1:c.296A>T	NP_001333020.1:p.Asp99Val
NM_001346092.1:c.161A>T	NP_001333021.1:p.Asp54Val
NR_144351.1:n.855-147A>T
NM_001065.4:c.620A>T MANE Select	NP_001056.1:p.Asp207Val
NM_001346091.2:c.296A>T	NP_001333020.1:p.Asp99Val
NM_001346092.2:c.161A>T	NP_001333021.1:p.Asp54Val
NR_144351.2:n.814-147A>T