Canonical Allele Identifier: CA478504919

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6442627G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6333461G>A , CM000674.2:g.6333461G>A	GRCh38
NC_000012.11:g.6442627G>A , CM000674.1:g.6442627G>A	GRCh37
NC_000012.10:g.6312888G>A	NCBI36
NG_007506.1:g.13635C>T , LRG_193:g.13635C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.412C>T
ENST00000437813.8:c.378C>T	ENSP00000513672.1:p.Gly126=
ENST00000440083.7:c.378C>T	ENSP00000413224.3:p.Gly126=
ENST00000535958.2:c.*205C>T	ENSP00000513673.1:n.*205C>T
ENST00000698339.1:c.378C>T	ENSP00000513670.1:p.Gly126=
ENST00000698340.1:c.378C>T	ENSP00000513671.1:p.Gly126=
ENST00000162749.7:c.378C>T MANE Select	ENSP00000162749.2:p.Gly126=
ENST00000162749.6:c.378C>T	ENSP00000162749.2:p.Gly126=
ENST00000366159.8:c.378C>T	ENSP00000380389.3:p.Gly126=
ENST00000437813.7:n.339C>T
ENST00000440083.6:c.378C>T	ENSP00000413224.2:p.Gly126=
ENST00000534885.5:c.224C>T	ENSP00000441803.1:p.Ala75Val
ENST00000536194.1:c.351C>T	ENSP00000442919.1:p.Gly117=
ENST00000539372.5:c.378C>T	ENSP00000442059.1:p.Gly126=
ENST00000540022.5:c.249C>T	ENSP00000438343.1:p.Gly83=
ENST00000543048.5:c.215-10C>T	ENSP00000439981.1:n.215-10C>T
ENST00000543995.5:c.194-10C>T	ENSP00000442405.1:n.194-10C>T
NM_001065.3:c.378C>T , LRG_193t1:c.378C>T	NP_001056.1:p.Gly126=
NM_001346091.1:c.54C>T	NP_001333020.1:p.Gly18=
NM_001346092.1:c.-200C>T	NP_001333021.1:n.-200C>T
NR_144351.1:n.681C>T
NM_001065.4:c.378C>T MANE Select	NP_001056.1:p.Gly126=
NM_001346091.2:c.54C>T	NP_001333020.1:p.Gly18=
NM_001346092.2:c.-200C>T	NP_001333021.1:n.-200C>T
NR_144351.2:n.640C>T