Canonical Allele Identifier: CA383547958

Gene: TNFRSF1A

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1721A>G
ENST00000437813.8:c.*81A>G	ENSP00000513672.1:n.*81A>G
ENST00000440083.7:c.839A>G	ENSP00000413224.3:p.Asp280Gly
ENST00000535038.2:n.802A>G
ENST00000535958.2:c.*447A>G	ENSP00000513673.1:n.*447A>G
ENST00000698337.1:n.469A>G
ENST00000698338.1:n.893A>G
ENST00000698339.1:c.*115A>G	ENSP00000513670.1:n.*115A>G
ENST00000698340.1:c.552-147A>G	ENSP00000513671.1:n.552-147A>G
ENST00000162749.7:c.620A>G MANE Select	ENSP00000162749.2:p.Asp207Gly
ENST00000162749.6:c.620A>G	ENSP00000162749.2:p.Asp207Gly
ENST00000534885.5:c.*97A>G	ENSP00000441803.1:n.*97A>G
ENST00000535038.1:n.290A>G
ENST00000536717.5:n.524A>G
ENST00000537842.5:n.224A>G
ENST00000539372.5:c.620A>G	ENSP00000442059.1:p.Asp207Gly
ENST00000540022.5:c.491A>G	ENSP00000438343.1:p.Asp164Gly
ENST00000543359.5:n.38-147A>G
ENST00000543995.5:c.*207A>G	ENSP00000442405.1:n.*207A>G
NM_001065.3:c.620A>G , LRG_193t1:c.620A>G	NP_001056.1:p.Asp207Gly
NM_001346091.1:c.296A>G	NP_001333020.1:p.Asp99Gly
NM_001346092.1:c.161A>G	NP_001333021.1:p.Asp54Gly
NR_144351.1:n.855-147A>G
NM_001065.4:c.620A>G MANE Select	NP_001056.1:p.Asp207Gly
NM_001346091.2:c.296A>G	NP_001333020.1:p.Asp99Gly
NM_001346092.2:c.161A>G	NP_001333021.1:p.Asp54Gly
NR_144351.2:n.814-147A>G