Canonical Allele Identifier: CA383549091

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6442281G>C (hg19) ; chr12:g.6333115G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6333115G>C , CM000674.2:g.6333115G>C	GRCh38
NC_000012.11:g.6442281G>C , CM000674.1:g.6442281G>C	GRCh37
NC_000012.10:g.6312542G>C	NCBI36
NG_007506.1:g.13981C>G , LRG_193:g.13981C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.539C>G
ENST00000437813.8:c.505C>G	ENSP00000513672.1:p.His169Asp
ENST00000440083.7:c.724C>G	ENSP00000413224.3:p.His242Asp
ENST00000535958.2:c.*332C>G	ENSP00000513673.1:n.*332C>G
ENST00000698339.1:c.505C>G	ENSP00000513670.1:p.His169Asp
ENST00000698340.1:c.505C>G	ENSP00000513671.1:p.His169Asp
ENST00000162749.7:c.505C>G MANE Select	ENSP00000162749.2:p.His169Asp
ENST00000162749.6:c.505C>G	ENSP00000162749.2:p.His169Asp
ENST00000366159.8:c.505C>G	ENSP00000380389.3:p.His169Asp
ENST00000437813.7:n.466C>G
ENST00000440083.6:c.724C>G	ENSP00000413224.2:p.His242Asp
ENST00000534885.5:c.351C>G	ENSP00000441803.1:p.Ala117=
ENST00000537842.5:n.109C>G
ENST00000539372.5:c.505C>G	ENSP00000442059.1:p.His169Asp
ENST00000540022.5:c.376C>G	ENSP00000438343.1:p.His126Asp
ENST00000543048.5:c.*116C>G	ENSP00000439981.1:n.*116C>G
ENST00000543995.5:c.*92C>G	ENSP00000442405.1:n.*92C>G
NM_001065.3:c.505C>G , LRG_193t1:c.505C>G	NP_001056.1:p.His169Asp
NM_001346091.1:c.181C>G	NP_001333020.1:p.His61Asp
NM_001346092.1:c.-73C>G	NP_001333021.1:n.-73C>G
NR_144351.1:n.808C>G
NM_001065.4:c.505C>G MANE Select	NP_001056.1:p.His169Asp
NM_001346091.2:c.181C>G	NP_001333020.1:p.His61Asp
NM_001346092.2:c.-73C>G	NP_001333021.1:n.-73C>G
NR_144351.2:n.767C>G