Canonical Allele Identifier: CA383547986

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6440030G>C (hg19) ; chr12:g.6330864G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330864G>C , CM000674.2:g.6330864G>C	GRCh38
NC_000012.11:g.6440030G>C , CM000674.1:g.6440030G>C	GRCh37
NC_000012.10:g.6310291G>C	NCBI36
NG_007506.1:g.16232C>G , LRG_193:g.16232C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1715C>G
ENST00000437813.8:c.*75C>G	ENSP00000513672.1:n.*75C>G
ENST00000440083.7:c.833C>G	ENSP00000413224.3:p.Thr278Ser
ENST00000535038.2:n.796C>G
ENST00000535958.2:c.*441C>G	ENSP00000513673.1:n.*441C>G
ENST00000698337.1:n.463C>G
ENST00000698338.1:n.887C>G
ENST00000698339.1:c.*109C>G	ENSP00000513670.1:n.*109C>G
ENST00000698340.1:c.552-153C>G	ENSP00000513671.1:n.552-153C>G
ENST00000162749.7:c.614C>G MANE Select	ENSP00000162749.2:p.Thr205Ser
ENST00000162749.6:c.614C>G	ENSP00000162749.2:p.Thr205Ser
ENST00000534885.5:c.*91C>G	ENSP00000441803.1:n.*91C>G
ENST00000535038.1:n.284C>G
ENST00000536717.5:n.518C>G
ENST00000537842.5:n.218C>G
ENST00000539372.5:c.614C>G	ENSP00000442059.1:p.Thr205Ser
ENST00000540022.5:c.485C>G	ENSP00000438343.1:p.Thr162Ser
ENST00000543359.5:n.38-153C>G
ENST00000543995.5:c.*201C>G	ENSP00000442405.1:n.*201C>G
NM_001065.3:c.614C>G , LRG_193t1:c.614C>G	NP_001056.1:p.Thr205Ser
NM_001346091.1:c.290C>G	NP_001333020.1:p.Thr97Ser
NM_001346092.1:c.155C>G	NP_001333021.1:p.Thr52Ser
NR_144351.1:n.855-153C>G
NM_001065.4:c.614C>G MANE Select	NP_001056.1:p.Thr205Ser
NM_001346091.2:c.290C>G	NP_001333020.1:p.Thr97Ser
NM_001346092.2:c.155C>G	NP_001333021.1:p.Thr52Ser
NR_144351.2:n.814-153C>G