Canonical Allele Identifier: CA383548177

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6440086C>G (hg19) ; chr12:g.6330920C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330920C>G , CM000674.2:g.6330920C>G	GRCh38
NC_000012.11:g.6440086C>G , CM000674.1:g.6440086C>G	GRCh37
NC_000012.10:g.6310347C>G	NCBI36
NG_007506.1:g.16176G>C , LRG_193:g.16176G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1659G>C
ENST00000437813.8:c.*19G>C	ENSP00000513672.1:n.*19G>C
ENST00000440083.7:c.777G>C	ENSP00000413224.3:p.Lys259Asn
ENST00000535038.2:n.740G>C
ENST00000535958.2:c.*385G>C	ENSP00000513673.1:n.*385G>C
ENST00000698337.1:n.407G>C
ENST00000698338.1:n.831G>C
ENST00000698339.1:c.*53G>C	ENSP00000513670.1:n.*53G>C
ENST00000698340.1:c.552-209G>C	ENSP00000513671.1:n.552-209G>C
ENST00000162749.7:c.558G>C MANE Select	ENSP00000162749.2:p.Lys186Asn
ENST00000162749.6:c.558G>C	ENSP00000162749.2:p.Lys186Asn
ENST00000534885.5:c.*35G>C	ENSP00000441803.1:n.*35G>C
ENST00000535038.1:n.228G>C
ENST00000536717.5:n.462G>C
ENST00000537842.5:n.162G>C
ENST00000539372.5:c.558G>C	ENSP00000442059.1:p.Lys186Asn
ENST00000540022.5:c.429G>C	ENSP00000438343.1:p.Lys143Asn
ENST00000543359.5:n.38-209G>C
ENST00000543995.5:c.*145G>C	ENSP00000442405.1:n.*145G>C
NM_001065.3:c.558G>C , LRG_193t1:c.558G>C	NP_001056.1:p.Lys186Asn
NM_001346091.1:c.234G>C	NP_001333020.1:p.Lys78Asn
NM_001346092.1:c.99G>C	NP_001333021.1:p.Lys33Asn
NR_144351.1:n.855-209G>C
NM_001065.4:c.558G>C MANE Select	NP_001056.1:p.Lys186Asn
NM_001346091.2:c.234G>C	NP_001333020.1:p.Lys78Asn
NM_001346092.2:c.99G>C	NP_001333021.1:p.Lys33Asn
NR_144351.2:n.814-209G>C