Canonical Allele Identifier: CA603483598

Gene: TNFRSF1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330717G>A , CM000674.2:g.6330717G>A	GRCh38
NC_000012.11:g.6439883G>A , CM000674.1:g.6439883G>A	GRCh37
NC_000012.10:g.6310144G>A	NCBI36
NG_007506.1:g.16379C>T , LRG_193:g.16379C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001065.4:c.626-6C>T MANE Select	NP_001056.1:n.626-6C>T
ENST00000162749.7:c.626-6C>T MANE Select	ENSP00000162749.2:n.626-6C>T
NM_001065.3:c.626-6C>T , LRG_193t1:c.626-6C>T	NP_001056.1:n.626-6C>T
NM_001346091.1:c.302-6C>T	NP_001333020.1:n.302-6C>T
NM_001346091.2:c.302-6C>T	NP_001333020.1:n.302-6C>T
NM_001346092.1:c.167-6C>T	NP_001333021.1:n.167-6C>T
NM_001346092.2:c.167-6C>T	NP_001333021.1:n.167-6C>T
NR_144351.1:n.855-6C>T
NR_144351.2:n.814-6C>T
ENST00000162749.6:c.626-6C>T	ENSP00000162749.2:n.626-6C>T
ENST00000366159.9:n.1727-6C>T
ENST00000437813.8:c.*87-6C>T	ENSP00000513672.1:n.*87-6C>T
ENST00000440083.7:c.845-6C>T	ENSP00000413224.3:n.845-6C>T
ENST00000534885.5:c.*103-6C>T	ENSP00000441803.1:n.*103-6C>T
ENST00000535038.1:n.431C>T
ENST00000535038.2:n.808-6C>T
ENST00000535958.2:c.*453-6C>T	ENSP00000513673.1:n.*453-6C>T
ENST00000536717.5:n.530-6C>T
ENST00000537842.5:n.230-6C>T
ENST00000539372.5:c.626-6C>T	ENSP00000442059.1:n.626-6C>T
ENST00000540022.5:c.497-6C>T	ENSP00000438343.1:n.497-6C>T
ENST00000543359.5:n.38-6C>T
ENST00000543995.5:c.*213-6C>T	ENSP00000442405.1:n.*213-6C>T
ENST00000698337.1:n.610C>T
ENST00000698338.1:n.1034C>T
ENST00000698339.1:c.*121-6C>T	ENSP00000513670.1:n.*121-6C>T
ENST00000698340.1:c.552-6C>T	ENSP00000513671.1:n.552-6C>T