Canonical Allele Identifier: CA383545625

Gene: TNFRSF1A

Linked Data

• gnomAD v4: 12-6329805-T-C
• MyVariant Identifiers: chr12:g.6438971T>C (hg19) ; chr12:g.6329805T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6329805T>C , CM000674.2:g.6329805T>C	GRCh38
NC_000012.11:g.6438971T>C , CM000674.1:g.6438971T>C	GRCh37
NC_000012.10:g.6309232T>C	NCBI36
NG_007506.1:g.17291A>G , LRG_193:g.17291A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000366159.9:n.2131A>G
ENST00000437813.8:c.*491A>G	ENSP00000513672.1:n.*491A>G
ENST00000440083.7:c.1249A>G	ENSP00000413224.3:p.Ser417Gly
ENST00000535958.2:c.*857A>G	ENSP00000513673.1:n.*857A>G
ENST00000698337.1:n.991A>G
ENST00000698338.1:n.1644A>G
ENST00000698339.1:c.*525A>G	ENSP00000513670.1:n.*525A>G
ENST00000698340.1:c.*269A>G	ENSP00000513671.1:n.*269A>G
ENST00000162749.7:c.1030A>G MANE Select	ENSP00000162749.2:p.Ser344Gly
ENST00000162749.6:c.1030A>G	ENSP00000162749.2:p.Ser344Gly
ENST00000534885.5:c.*507A>G	ENSP00000441803.1:n.*507A>G
ENST00000536717.5:n.934A>G
ENST00000540022.5:c.901A>G	ENSP00000438343.1:p.Ser301Gly
ENST00000543359.5:n.442A>G
ENST00000543995.5:c.*617A>G	ENSP00000442405.1:n.*617A>G
NM_001065.3:c.1030A>G , LRG_193t1:c.1030A>G	NP_001056.1:p.Ser344Gly
NM_001346091.1:c.706A>G	NP_001333020.1:p.Ser236Gly
NM_001346092.1:c.571A>G	NP_001333021.1:p.Ser191Gly
NR_144351.1:n.1259A>G
NM_001065.4:c.1030A>G MANE Select	NP_001056.1:p.Ser344Gly
NM_001346091.2:c.706A>G	NP_001333020.1:p.Ser236Gly
NM_001346092.2:c.571A>G	NP_001333021.1:p.Ser191Gly
NR_144351.2:n.1218A>G