Canonical Allele Identifier: CA383551742

Gene: TNFRSF1A

Linked Data

• dbSNP Id: rs1592053686
• gnomAD v4: 12-6341792-T-G
• MyVariant Identifiers: chr12:g.6450958T>G (hg19) ; chr12:g.6341792T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6341792T>G , CM000674.2:g.6341792T>G	GRCh38
NC_000012.11:g.6450958T>G , CM000674.1:g.6450958T>G	GRCh37
NC_000012.10:g.6321219T>G	NCBI36
NG_007506.1:g.5304A>C , LRG_193:g.5304A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000366159.9:n.57A>C
ENST00000437813.8:c.23A>C	ENSP00000513672.1:p.Asp8Ala
ENST00000440083.7:c.23A>C	ENSP00000413224.3:p.Asp8Ala
ENST00000535958.2:c.23A>C	ENSP00000513673.1:p.Asp8Ala
ENST00000698339.1:c.23A>C	ENSP00000513670.1:p.Asp8Ala
ENST00000698340.1:c.23A>C	ENSP00000513671.1:p.Asp8Ala
ENST00000162749.7:c.23A>C MANE Select	ENSP00000162749.2:p.Asp8Ala
ENST00000162749.6:c.23A>C	ENSP00000162749.2:p.Asp8Ala
ENST00000366159.8:c.23A>C	ENSP00000380389.3:p.Asp8Ala
ENST00000440083.6:c.23A>C	ENSP00000413224.2:p.Asp8Ala
ENST00000534885.5:c.23A>C	ENSP00000441803.1:p.Asp8Ala
ENST00000535958.1:n.244A>C
ENST00000536194.1:c.23A>C	ENSP00000442919.1:p.Asp8Ala
ENST00000538363.1:n.213A>C
ENST00000539372.5:c.23A>C	ENSP00000442059.1:p.Asp8Ala
ENST00000540022.5:c.23A>C	ENSP00000438343.1:p.Asp8Ala
ENST00000543048.5:c.23A>C	ENSP00000439981.1:p.Asp8Ala
ENST00000543995.5:c.23A>C	ENSP00000442405.1:p.Asp8Ala
NM_001065.3:c.23A>C , LRG_193t1:c.23A>C	NP_001056.1:p.Asp8Ala
NM_001346091.1:c.-148A>C	NP_001333020.1:n.-148A>C
NM_001346092.1:c.-555A>C	NP_001333021.1:n.-555A>C
NR_144351.1:n.326A>C
NM_001065.4:c.23A>C MANE Select	NP_001056.1:p.Asp8Ala
NM_001346091.2:c.-148A>C	NP_001333020.1:n.-148A>C
NM_001346092.2:c.-555A>C	NP_001333021.1:n.-555A>C
NR_144351.2:n.285A>C