Canonical Allele Identifier: CA478113999

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6450945T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6341779T>G , CM000674.2:g.6341779T>G	GRCh38
NC_000012.11:g.6450945T>G , CM000674.1:g.6450945T>G	GRCh37
NC_000012.10:g.6321206T>G	NCBI36
NG_007506.1:g.5317A>C , LRG_193:g.5317A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000366159.9:n.70A>C
ENST00000437813.8:c.36A>C	ENSP00000513672.1:p.Pro12=
ENST00000440083.7:c.36A>C	ENSP00000413224.3:p.Pro12=
ENST00000535958.2:c.36A>C	ENSP00000513673.1:p.Pro12=
ENST00000698339.1:c.36A>C	ENSP00000513670.1:p.Pro12=
ENST00000698340.1:c.36A>C	ENSP00000513671.1:p.Pro12=
ENST00000162749.7:c.36A>C MANE Select	ENSP00000162749.2:p.Pro12=
ENST00000162749.6:c.36A>C	ENSP00000162749.2:p.Pro12=
ENST00000366159.8:c.36A>C	ENSP00000380389.3:p.Pro12=
ENST00000440083.6:c.36A>C	ENSP00000413224.2:p.Pro12=
ENST00000534885.5:c.36A>C	ENSP00000441803.1:p.Pro12=
ENST00000535958.1:n.257A>C
ENST00000536194.1:c.36A>C	ENSP00000442919.1:p.Pro12=
ENST00000538363.1:n.226A>C
ENST00000539372.5:c.36A>C	ENSP00000442059.1:p.Pro12=
ENST00000540022.5:c.36A>C	ENSP00000438343.1:p.Pro12=
ENST00000543048.5:c.36A>C	ENSP00000439981.1:p.Pro12=
ENST00000543995.5:c.36A>C	ENSP00000442405.1:p.Pro12=
NM_001065.3:c.36A>C , LRG_193t1:c.36A>C	NP_001056.1:p.Pro12=
NM_001346091.1:c.-135A>C	NP_001333020.1:n.-135A>C
NM_001346092.1:c.-542A>C	NP_001333021.1:n.-542A>C
NR_144351.1:n.339A>C
NM_001065.4:c.36A>C MANE Select	NP_001056.1:p.Pro12=
NM_001346091.2:c.-135A>C	NP_001333020.1:n.-135A>C
NM_001346092.2:c.-542A>C	NP_001333021.1:n.-542A>C
NR_144351.2:n.298A>C