Canonical Allele Identifier: CA478504798

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6439077C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6329911C>G , CM000674.2:g.6329911C>G	GRCh38
NC_000012.11:g.6439077C>G , CM000674.1:g.6439077C>G	GRCh37
NC_000012.10:g.6309338C>G	NCBI36
NG_007506.1:g.17185G>C , LRG_193:g.17185G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000366159.9:n.2025G>C
ENST00000437813.8:c.*385G>C	ENSP00000513672.1:n.*385G>C
ENST00000440083.7:c.1143G>C	ENSP00000413224.3:p.Ala381=
ENST00000535958.2:c.*751G>C	ENSP00000513673.1:n.*751G>C
ENST00000698337.1:n.885G>C
ENST00000698338.1:n.1538G>C
ENST00000698339.1:c.*419G>C	ENSP00000513670.1:n.*419G>C
ENST00000698340.1:c.*163G>C	ENSP00000513671.1:n.*163G>C
ENST00000162749.7:c.924G>C MANE Select	ENSP00000162749.2:p.Ala308=
ENST00000162749.6:c.924G>C	ENSP00000162749.2:p.Ala308=
ENST00000534885.5:c.*401G>C	ENSP00000441803.1:n.*401G>C
ENST00000536717.5:n.828G>C
ENST00000537842.5:n.373-12G>C
ENST00000540022.5:c.795G>C	ENSP00000438343.1:p.Ala265=
ENST00000543359.5:n.336G>C
ENST00000543995.5:c.*511G>C	ENSP00000442405.1:n.*511G>C
NM_001065.3:c.924G>C , LRG_193t1:c.924G>C	NP_001056.1:p.Ala308=
NM_001346091.1:c.600G>C	NP_001333020.1:p.Ala200=
NM_001346092.1:c.465G>C	NP_001333021.1:p.Ala155=
NR_144351.1:n.1153G>C
NM_001065.4:c.924G>C MANE Select	NP_001056.1:p.Ala308=
NM_001346091.2:c.600G>C	NP_001333020.1:p.Ala200=
NM_001346092.2:c.465G>C	NP_001333021.1:p.Ala155=
NR_144351.2:n.1112G>C