Canonical Allele Identifier: CA383548004

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6440035C>G (hg19) ; chr12:g.6330869C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330869C>G , CM000674.2:g.6330869C>G	GRCh38
NC_000012.11:g.6440035C>G , CM000674.1:g.6440035C>G	GRCh37
NC_000012.10:g.6310296C>G	NCBI36
NG_007506.1:g.16227G>C , LRG_193:g.16227G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1710G>C
ENST00000437813.8:c.*70G>C	ENSP00000513672.1:n.*70G>C
ENST00000440083.7:c.828G>C	ENSP00000413224.3:p.Lys276Asn
ENST00000535038.2:n.791G>C
ENST00000535958.2:c.*436G>C	ENSP00000513673.1:n.*436G>C
ENST00000698337.1:n.458G>C
ENST00000698338.1:n.882G>C
ENST00000698339.1:c.*104G>C	ENSP00000513670.1:n.*104G>C
ENST00000698340.1:c.552-158G>C	ENSP00000513671.1:n.552-158G>C
ENST00000162749.7:c.609G>C MANE Select	ENSP00000162749.2:p.Lys203Asn
ENST00000162749.6:c.609G>C	ENSP00000162749.2:p.Lys203Asn
ENST00000534885.5:c.*86G>C	ENSP00000441803.1:n.*86G>C
ENST00000535038.1:n.279G>C
ENST00000536717.5:n.513G>C
ENST00000537842.5:n.213G>C
ENST00000539372.5:c.609G>C	ENSP00000442059.1:p.Lys203Asn
ENST00000540022.5:c.480G>C	ENSP00000438343.1:p.Lys160Asn
ENST00000543359.5:n.38-158G>C
ENST00000543995.5:c.*196G>C	ENSP00000442405.1:n.*196G>C
NM_001065.3:c.609G>C , LRG_193t1:c.609G>C	NP_001056.1:p.Lys203Asn
NM_001346091.1:c.285G>C	NP_001333020.1:p.Lys95Asn
NM_001346092.1:c.150G>C	NP_001333021.1:p.Lys50Asn
NR_144351.1:n.855-158G>C
NM_001065.4:c.609G>C MANE Select	NP_001056.1:p.Lys203Asn
NM_001346091.2:c.285G>C	NP_001333020.1:p.Lys95Asn
NM_001346092.2:c.150G>C	NP_001333021.1:p.Lys50Asn
NR_144351.2:n.814-158G>C