Canonical Allele Identifier: CA478112503

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6439846G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330680G>A , CM000674.2:g.6330680G>A	GRCh38
NC_000012.11:g.6439846G>A , CM000674.1:g.6439846G>A	GRCh37
NC_000012.10:g.6310107G>A	NCBI36
NG_007506.1:g.16416C>T , LRG_193:g.16416C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1758C>T
ENST00000437813.8:c.*118C>T	ENSP00000513672.1:n.*118C>T
ENST00000440083.7:c.876C>T	ENSP00000413224.3:p.Phe292=
ENST00000535038.2:n.839C>T
ENST00000535958.2:c.*484C>T	ENSP00000513673.1:n.*484C>T
ENST00000698337.1:n.647C>T
ENST00000698338.1:n.1071C>T
ENST00000698339.1:c.*152C>T	ENSP00000513670.1:n.*152C>T
ENST00000698340.1:c.583C>T	ENSP00000513671.1:p.Leu195Phe
ENST00000162749.7:c.657C>T MANE Select	ENSP00000162749.2:p.Phe219=
ENST00000162749.6:c.657C>T	ENSP00000162749.2:p.Phe219=
ENST00000534885.5:c.*134C>T	ENSP00000441803.1:n.*134C>T
ENST00000535038.1:n.468C>T
ENST00000536717.5:n.561C>T
ENST00000537842.5:n.261C>T
ENST00000539372.5:c.657C>T	ENSP00000442059.1:p.Phe219=
ENST00000540022.5:c.528C>T	ENSP00000438343.1:p.Phe176=
ENST00000543359.5:n.69C>T
ENST00000543995.5:c.*244C>T	ENSP00000442405.1:n.*244C>T
NM_001065.3:c.657C>T , LRG_193t1:c.657C>T	NP_001056.1:p.Phe219=
NM_001346091.1:c.333C>T	NP_001333020.1:p.Phe111=
NM_001346092.1:c.198C>T	NP_001333021.1:p.Phe66=
NR_144351.1:n.886C>T
NM_001065.4:c.657C>T MANE Select	NP_001056.1:p.Phe219=
NM_001346091.2:c.333C>T	NP_001333020.1:p.Phe111=
NM_001346092.2:c.198C>T	NP_001333021.1:p.Phe66=
NR_144351.2:n.845C>T