Canonical Allele Identifier: CA478112687

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6440020T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330854T>G , CM000674.2:g.6330854T>G	GRCh38
NC_000012.11:g.6440020T>G , CM000674.1:g.6440020T>G	GRCh37
NC_000012.10:g.6310281T>G	NCBI36
NG_007506.1:g.16242A>C , LRG_193:g.16242A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1725A>C
ENST00000437813.8:c.*85A>C	ENSP00000513672.1:n.*85A>C
ENST00000440083.7:c.843A>C	ENSP00000413224.3:p.Ser281=
ENST00000535038.2:n.806A>C
ENST00000535958.2:c.*451A>C	ENSP00000513673.1:n.*451A>C
ENST00000698337.1:n.473A>C
ENST00000698338.1:n.897A>C
ENST00000698339.1:c.*119A>C	ENSP00000513670.1:n.*119A>C
ENST00000698340.1:c.552-143A>C	ENSP00000513671.1:n.552-143A>C
ENST00000162749.7:c.624A>C MANE Select	ENSP00000162749.2:p.Ser208=
ENST00000162749.6:c.624A>C	ENSP00000162749.2:p.Ser208=
ENST00000534885.5:c.*101A>C	ENSP00000441803.1:n.*101A>C
ENST00000535038.1:n.294A>C
ENST00000536717.5:n.528A>C
ENST00000537842.5:n.228A>C
ENST00000539372.5:c.624A>C	ENSP00000442059.1:p.Ser208=
ENST00000540022.5:c.495A>C	ENSP00000438343.1:p.Ser165=
ENST00000543359.5:n.38-143A>C
ENST00000543995.5:c.*211A>C	ENSP00000442405.1:n.*211A>C
NM_001065.3:c.624A>C , LRG_193t1:c.624A>C	NP_001056.1:p.Ser208=
NM_001346091.1:c.300A>C	NP_001333020.1:p.Ser100=
NM_001346092.1:c.165A>C	NP_001333021.1:p.Ser55=
NR_144351.1:n.855-143A>C
NM_001065.4:c.624A>C MANE Select	NP_001056.1:p.Ser208=
NM_001346091.2:c.300A>C	NP_001333020.1:p.Ser100=
NM_001346092.2:c.165A>C	NP_001333021.1:p.Ser55=
NR_144351.2:n.814-143A>C