Canonical Allele Identifier: CA383548020

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6440042T>G (hg19) ; chr12:g.6330876T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330876T>G , CM000674.2:g.6330876T>G	GRCh38
NC_000012.11:g.6440042T>G , CM000674.1:g.6440042T>G	GRCh37
NC_000012.10:g.6310303T>G	NCBI36
NG_007506.1:g.16220A>C , LRG_193:g.16220A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1703A>C
ENST00000437813.8:c.*63A>C	ENSP00000513672.1:n.*63A>C
ENST00000440083.7:c.821A>C	ENSP00000413224.3:p.Asn274Thr
ENST00000535038.2:n.784A>C
ENST00000535958.2:c.*429A>C	ENSP00000513673.1:n.*429A>C
ENST00000698337.1:n.451A>C
ENST00000698338.1:n.875A>C
ENST00000698339.1:c.*97A>C	ENSP00000513670.1:n.*97A>C
ENST00000698340.1:c.552-165A>C	ENSP00000513671.1:n.552-165A>C
ENST00000162749.7:c.602A>C MANE Select	ENSP00000162749.2:p.Asn201Thr
ENST00000162749.6:c.602A>C	ENSP00000162749.2:p.Asn201Thr
ENST00000534885.5:c.*79A>C	ENSP00000441803.1:n.*79A>C
ENST00000535038.1:n.272A>C
ENST00000536717.5:n.506A>C
ENST00000537842.5:n.206A>C
ENST00000539372.5:c.602A>C	ENSP00000442059.1:p.Asn201Thr
ENST00000540022.5:c.473A>C	ENSP00000438343.1:p.Asn158Thr
ENST00000543359.5:n.38-165A>C
ENST00000543995.5:c.*189A>C	ENSP00000442405.1:n.*189A>C
NM_001065.3:c.602A>C , LRG_193t1:c.602A>C	NP_001056.1:p.Asn201Thr
NM_001346091.1:c.278A>C	NP_001333020.1:p.Asn93Thr
NM_001346092.1:c.143A>C	NP_001333021.1:p.Asn48Thr
NR_144351.1:n.855-165A>C
NM_001065.4:c.602A>C MANE Select	NP_001056.1:p.Asn201Thr
NM_001346091.2:c.278A>C	NP_001333020.1:p.Asn93Thr
NM_001346092.2:c.143A>C	NP_001333021.1:p.Asn48Thr
NR_144351.2:n.814-165A>C