Canonical Allele Identifier: CA2617256043

Gene: TNFRSF1A

Linked Data

• gnomAD v4: 12-6334081-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6334081T>C , CM000674.2:g.6334081T>C	GRCh38
NC_000012.11:g.6443247T>C , CM000674.1:g.6443247T>C	GRCh37
NC_000012.10:g.6313508T>C	NCBI36
NG_007506.1:g.13015A>G , LRG_193:g.13015A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.227+10A>G
ENST00000437813.8:c.193+10A>G	ENSP00000513672.1:n.193+10A>G
ENST00000440083.7:c.193+10A>G	ENSP00000413224.3:n.193+10A>G
ENST00000535958.2:c.193+10A>G	ENSP00000513673.1:n.193+10A>G
ENST00000698339.1:c.193+10A>G	ENSP00000513670.1:n.193+10A>G
ENST00000698340.1:c.193+10A>G	ENSP00000513671.1:n.193+10A>G
ENST00000162749.7:c.193+10A>G MANE Select	ENSP00000162749.2:n.193+10A>G
ENST00000162749.6:c.193+10A>G	ENSP00000162749.2:n.193+10A>G
ENST00000366159.8:c.193+10A>G	ENSP00000380389.3:n.193+10A>G
ENST00000437813.7:n.154+10A>G
ENST00000440083.6:c.193+10A>G	ENSP00000413224.2:n.193+10A>G
ENST00000534885.5:c.40-216A>G	ENSP00000441803.1:n.40-216A>G
ENST00000535958.1:n.414+10A>G
ENST00000536194.1:c.193+10A>G	ENSP00000442919.1:n.193+10A>G
ENST00000538363.1:n.393A>G
ENST00000539372.5:c.193+10A>G	ENSP00000442059.1:n.193+10A>G
ENST00000540022.5:c.193+10A>G	ENSP00000438343.1:n.193+10A>G
ENST00000543048.5:c.193+10A>G	ENSP00000439981.1:n.193+10A>G
ENST00000543995.5:c.193+10A>G	ENSP00000442405.1:n.193+10A>G
NM_001065.3:c.193+10A>G , LRG_193t1:c.193+10A>G	NP_001056.1:n.193+10A>G
NM_001346091.1:c.-131-216A>G	NP_001333020.1:n.-131-216A>G
NM_001346092.1:c.-385+10A>G	NP_001333021.1:n.-385+10A>G
NR_144351.1:n.496+10A>G
NM_001065.4:c.193+10A>G MANE Select	NP_001056.1:n.193+10A>G
NM_001346091.2:c.-131-216A>G	NP_001333020.1:n.-131-216A>G
NM_001346092.2:c.-385+10A>G	NP_001333021.1:n.-385+10A>G
NR_144351.2:n.455+10A>G