Canonical Allele Identifier: CA478505021
Gene: TNFRSF1A HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.6443267C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6334101C>T , CM000674.2:g.6334101C>T GRCh38
NC_000012.11:g.6443267C>T , CM000674.1:g.6443267C>T GRCh37
NC_000012.10:g.6313528C>T NCBI36
NG_007506.1:g.12995G>A , LRG_193:g.12995G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000366159.9:n.217G>A
ENST00000437813.8:c.183G>A ENSP00000513672.1:p.Lys61=
ENST00000440083.7:c.183G>A ENSP00000413224.3:p.Lys61=
ENST00000535958.2:c.183G>A ENSP00000513673.1:p.Lys61=
ENST00000698339.1:c.183G>A ENSP00000513670.1:p.Lys61=
ENST00000698340.1:c.183G>A ENSP00000513671.1:p.Lys61=
ENST00000162749.7:c.183G>A MANE Select ENSP00000162749.2:p.Lys61=
ENST00000162749.6:c.183G>A ENSP00000162749.2:p.Lys61=
ENST00000366159.8:c.183G>A ENSP00000380389.3:p.Lys61=
ENST00000437813.7:n.144G>A
ENST00000440083.6:c.183G>A ENSP00000413224.2:p.Lys61=
ENST00000534885.5:c.40-236G>A ENSP00000441803.1:n.40-236G>A
ENST00000535958.1:n.404G>A
ENST00000536194.1:c.183G>A ENSP00000442919.1:p.Lys61=
ENST00000538363.1:n.373G>A
ENST00000539372.5:c.183G>A ENSP00000442059.1:p.Lys61=
ENST00000540022.5:c.183G>A ENSP00000438343.1:p.Lys61=
ENST00000543048.5:c.183G>A ENSP00000439981.1:p.Lys61=
ENST00000543995.5:c.183G>A ENSP00000442405.1:p.Lys61=
NM_001065.3:c.183G>A , LRG_193t1:c.183G>A NP_001056.1:p.Lys61=
NM_001346091.1:c.-131-236G>A NP_001333020.1:n.-131-236G>A
NM_001346092.1:c.-395G>A NP_001333021.1:n.-395G>A
NR_144351.1:n.486G>A
NM_001065.4:c.183G>A MANE Select NP_001056.1:p.Lys61=
NM_001346091.2:c.-131-236G>A NP_001333020.1:n.-131-236G>A
NM_001346092.2:c.-395G>A NP_001333021.1:n.-395G>A
NR_144351.2:n.445G>A