Canonical Allele Identifier: CA478504772

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6438990G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6329824G>A , CM000674.2:g.6329824G>A	GRCh38
NC_000012.11:g.6438990G>A , CM000674.1:g.6438990G>A	GRCh37
NC_000012.10:g.6309251G>A	NCBI36
NG_007506.1:g.17272C>T , LRG_193:g.17272C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.2112C>T
ENST00000437813.8:c.*472C>T	ENSP00000513672.1:n.*472C>T
ENST00000440083.7:c.1230C>T	ENSP00000413224.3:p.Pro410=
ENST00000535958.2:c.*838C>T	ENSP00000513673.1:n.*838C>T
ENST00000698337.1:n.972C>T
ENST00000698338.1:n.1625C>T
ENST00000698339.1:c.*506C>T	ENSP00000513670.1:n.*506C>T
ENST00000698340.1:c.*250C>T	ENSP00000513671.1:n.*250C>T
ENST00000162749.7:c.1011C>T MANE Select	ENSP00000162749.2:p.Pro337=
ENST00000162749.6:c.1011C>T	ENSP00000162749.2:p.Pro337=
ENST00000534885.5:c.*488C>T	ENSP00000441803.1:n.*488C>T
ENST00000536717.5:n.915C>T
ENST00000540022.5:c.882C>T	ENSP00000438343.1:p.Pro294=
ENST00000543359.5:n.423C>T
ENST00000543995.5:c.*598C>T	ENSP00000442405.1:n.*598C>T
NM_001065.3:c.1011C>T , LRG_193t1:c.1011C>T	NP_001056.1:p.Pro337=
NM_001346091.1:c.687C>T	NP_001333020.1:p.Pro229=
NM_001346092.1:c.552C>T	NP_001333021.1:p.Pro184=
NR_144351.1:n.1240C>T
NM_001065.4:c.1011C>T MANE Select	NP_001056.1:p.Pro337=
NM_001346091.2:c.687C>T	NP_001333020.1:p.Pro229=
NM_001346092.2:c.552C>T	NP_001333021.1:p.Pro184=
NR_144351.2:n.1199C>T