Canonical Allele Identifier: CA232325417

Gene: TNFRSF1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6329248A>G , CM000674.2:g.6329248A>G	GRCh38
NC_000012.11:g.6438414A>G , CM000674.1:g.6438414A>G	GRCh37
NC_000012.10:g.6308675A>G	NCBI36
NG_007506.1:g.17848T>C , LRG_193:g.17848T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001065.4:c.*64T>C MANE Select	NP_001056.1:n.*64T>C
ENST00000162749.7:c.*64T>C MANE Select	ENSP00000162749.2:n.*64T>C
NM_001065.3:c.*64T>C , LRG_193t1:c.*64T>C	NP_001056.1:n.*64T>C
NM_001346091.1:c.*64T>C	NP_001333020.1:n.*64T>C
NM_001346091.2:c.*64T>C	NP_001333020.1:n.*64T>C
NM_001346092.1:c.*64T>C	NP_001333021.1:n.*64T>C
NM_001346092.2:c.*64T>C	NP_001333021.1:n.*64T>C
NR_144351.1:n.1661T>C
NR_144351.2:n.1620T>C
ENST00000162749.6:c.*64T>C	ENSP00000162749.2:n.*64T>C
ENST00000366159.9:n.2533T>C
ENST00000437813.8:c.*893T>C	ENSP00000513672.1:n.*893T>C
ENST00000440083.7:c.*64T>C	ENSP00000413224.3:n.*64T>C
ENST00000534885.5:c.*909T>C	ENSP00000441803.1:n.*909T>C
ENST00000535958.2:c.*1259T>C	ENSP00000513673.1:n.*1259T>C
ENST00000536717.5:n.1336T>C
ENST00000540022.5:c.*64T>C	ENSP00000438343.1:n.*64T>C
ENST00000543995.5:c.*1019T>C	ENSP00000442405.1:n.*1019T>C
ENST00000698337.1:n.1393T>C
ENST00000698338.1:n.2046T>C
ENST00000698339.1:c.*927T>C	ENSP00000513670.1:n.*927T>C
ENST00000698340.1:c.*671T>C	ENSP00000513671.1:n.*671T>C