Canonical Allele Identifier: CA383548037

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6440049T>A (hg19) ; chr12:g.6330883T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330883T>A , CM000674.2:g.6330883T>A	GRCh38
NC_000012.11:g.6440049T>A , CM000674.1:g.6440049T>A	GRCh37
NC_000012.10:g.6310310T>A	NCBI36
NG_007506.1:g.16213A>T , LRG_193:g.16213A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1696A>T
ENST00000437813.8:c.*56A>T	ENSP00000513672.1:n.*56A>T
ENST00000440083.7:c.814A>T	ENSP00000413224.3:p.Ile272Phe
ENST00000535038.2:n.777A>T
ENST00000535958.2:c.*422A>T	ENSP00000513673.1:n.*422A>T
ENST00000698337.1:n.444A>T
ENST00000698338.1:n.868A>T
ENST00000698339.1:c.*90A>T	ENSP00000513670.1:n.*90A>T
ENST00000698340.1:c.552-172A>T	ENSP00000513671.1:n.552-172A>T
ENST00000162749.7:c.595A>T MANE Select	ENSP00000162749.2:p.Ile199Phe
ENST00000162749.6:c.595A>T	ENSP00000162749.2:p.Ile199Phe
ENST00000534885.5:c.*72A>T	ENSP00000441803.1:n.*72A>T
ENST00000535038.1:n.265A>T
ENST00000536717.5:n.499A>T
ENST00000537842.5:n.199A>T
ENST00000539372.5:c.595A>T	ENSP00000442059.1:p.Ile199Phe
ENST00000540022.5:c.466A>T	ENSP00000438343.1:p.Ile156Phe
ENST00000543359.5:n.38-172A>T
ENST00000543995.5:c.*182A>T	ENSP00000442405.1:n.*182A>T
NM_001065.3:c.595A>T , LRG_193t1:c.595A>T	NP_001056.1:p.Ile199Phe
NM_001346091.1:c.271A>T	NP_001333020.1:p.Ile91Phe
NM_001346092.1:c.136A>T	NP_001333021.1:p.Ile46Phe
NR_144351.1:n.855-172A>T
NM_001065.4:c.595A>T MANE Select	NP_001056.1:p.Ile199Phe
NM_001346091.2:c.271A>T	NP_001333020.1:p.Ile91Phe
NM_001346092.2:c.136A>T	NP_001333021.1:p.Ile46Phe
NR_144351.2:n.814-172A>T