Canonical Allele Identifier: CA383549138

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6442301T>G (hg19) ; chr12:g.6333135T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6333135T>G , CM000674.2:g.6333135T>G	GRCh38
NC_000012.11:g.6442301T>G , CM000674.1:g.6442301T>G	GRCh37
NC_000012.10:g.6312562T>G	NCBI36
NG_007506.1:g.13961A>C , LRG_193:g.13961A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.519A>C
ENST00000437813.8:c.485A>C	ENSP00000513672.1:p.Gln162Pro
ENST00000440083.7:c.704A>C	ENSP00000413224.3:p.Gln235Pro
ENST00000535958.2:c.*312A>C	ENSP00000513673.1:n.*312A>C
ENST00000698339.1:c.485A>C	ENSP00000513670.1:p.Gln162Pro
ENST00000698340.1:c.485A>C	ENSP00000513671.1:p.Gln162Pro
ENST00000162749.7:c.485A>C MANE Select	ENSP00000162749.2:p.Gln162Pro
ENST00000162749.6:c.485A>C	ENSP00000162749.2:p.Gln162Pro
ENST00000366159.8:c.485A>C	ENSP00000380389.3:p.Gln162Pro
ENST00000437813.7:n.446A>C
ENST00000440083.6:c.704A>C	ENSP00000413224.2:p.Gln235Pro
ENST00000534885.5:c.331A>C	ENSP00000441803.1:p.Arg111=
ENST00000537842.5:n.89A>C
ENST00000539372.5:c.485A>C	ENSP00000442059.1:p.Gln162Pro
ENST00000540022.5:c.356A>C	ENSP00000438343.1:p.Gln119Pro
ENST00000543048.5:c.*96A>C	ENSP00000439981.1:n.*96A>C
ENST00000543995.5:c.*72A>C	ENSP00000442405.1:n.*72A>C
NM_001065.3:c.485A>C , LRG_193t1:c.485A>C	NP_001056.1:p.Gln162Pro
NM_001346091.1:c.161A>C	NP_001333020.1:p.Gln54Pro
NM_001346092.1:c.-93A>C	NP_001333021.1:n.-93A>C
NR_144351.1:n.788A>C
NM_001065.4:c.485A>C MANE Select	NP_001056.1:p.Gln162Pro
NM_001346091.2:c.161A>C	NP_001333020.1:p.Gln54Pro
NM_001346092.2:c.-93A>C	NP_001333021.1:n.-93A>C
NR_144351.2:n.747A>C