Canonical Allele Identifier: CA690834023

Gene: TNFRSF1A

Linked Data

• dbSNP Id: rs933262503
• gnomAD v3: 12-6339988-A-G
• gnomAD v4: 12-6339988-A-G
• MyVariant Identifiers: chr12:g.6449154A>G (hg19) ; chr12:g.6339988A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6339988A>G , CM000674.2:g.6339988A>G	GRCh38
NC_000012.11:g.6449154A>G , CM000674.1:g.6449154A>G	GRCh37
NC_000012.10:g.6319415A>G	NCBI36
NG_007506.1:g.7108T>C , LRG_193:g.7108T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000366159.9:n.73+1788T>C
ENST00000437813.8:c.39+1788T>C	ENSP00000513672.1:n.39+1788T>C
ENST00000440083.7:c.39+1788T>C	ENSP00000413224.3:n.39+1788T>C
ENST00000535958.2:c.39+1788T>C	ENSP00000513673.1:n.39+1788T>C
ENST00000698339.1:c.39+1788T>C	ENSP00000513670.1:n.39+1788T>C
ENST00000698340.1:c.39+1788T>C	ENSP00000513671.1:n.39+1788T>C
ENST00000162749.7:c.39+1788T>C MANE Select	ENSP00000162749.2:n.39+1788T>C
ENST00000162749.6:c.39+1788T>C	ENSP00000162749.2:n.39+1788T>C
ENST00000366159.8:c.39+1788T>C	ENSP00000380389.3:n.39+1788T>C
ENST00000440083.6:c.39+1788T>C	ENSP00000413224.2:n.39+1788T>C
ENST00000534885.5:c.39+1788T>C	ENSP00000441803.1:n.39+1788T>C
ENST00000535958.1:n.260+1788T>C
ENST00000536194.1:c.39+1788T>C	ENSP00000442919.1:n.39+1788T>C
ENST00000538363.1:n.229+1788T>C
ENST00000539372.5:c.39+1788T>C	ENSP00000442059.1:n.39+1788T>C
ENST00000540022.5:c.39+1788T>C	ENSP00000438343.1:n.39+1788T>C
ENST00000543048.5:c.39+1788T>C	ENSP00000439981.1:n.39+1788T>C
ENST00000543995.5:c.39+1788T>C	ENSP00000442405.1:n.39+1788T>C
NM_001065.3:c.39+1788T>C , LRG_193t1:c.39+1788T>C	NP_001056.1:n.39+1788T>C
NM_001346091.1:c.-132+1788T>C	NP_001333020.1:n.-132+1788T>C
NM_001346092.1:c.-539+1788T>C	NP_001333021.1:n.-539+1788T>C
NR_144351.1:n.342+1788T>C
NM_001065.4:c.39+1788T>C MANE Select	NP_001056.1:n.39+1788T>C
NM_001346091.2:c.-132+1788T>C	NP_001333020.1:n.-132+1788T>C
NM_001346092.2:c.-539+1788T>C	NP_001333021.1:n.-539+1788T>C
NR_144351.2:n.301+1788T>C