Canonical Allele Identifier: CA383545628

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6438972G>T (hg19) ; chr12:g.6329806G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6329806G>T , CM000674.2:g.6329806G>T	GRCh38
NC_000012.11:g.6438972G>T , CM000674.1:g.6438972G>T	GRCh37
NC_000012.10:g.6309233G>T	NCBI36
NG_007506.1:g.17290C>A , LRG_193:g.17290C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000366159.9:n.2130C>A
ENST00000437813.8:c.*490C>A	ENSP00000513672.1:n.*490C>A
ENST00000440083.7:c.1248C>A	ENSP00000413224.3:p.Asp416Glu
ENST00000535958.2:c.*856C>A	ENSP00000513673.1:n.*856C>A
ENST00000698337.1:n.990C>A
ENST00000698338.1:n.1643C>A
ENST00000698339.1:c.*524C>A	ENSP00000513670.1:n.*524C>A
ENST00000698340.1:c.*268C>A	ENSP00000513671.1:n.*268C>A
ENST00000162749.7:c.1029C>A MANE Select	ENSP00000162749.2:p.Asp343Glu
ENST00000162749.6:c.1029C>A	ENSP00000162749.2:p.Asp343Glu
ENST00000534885.5:c.*506C>A	ENSP00000441803.1:n.*506C>A
ENST00000536717.5:n.933C>A
ENST00000540022.5:c.900C>A	ENSP00000438343.1:p.Asp300Glu
ENST00000543359.5:n.441C>A
ENST00000543995.5:c.*616C>A	ENSP00000442405.1:n.*616C>A
NM_001065.3:c.1029C>A , LRG_193t1:c.1029C>A	NP_001056.1:p.Asp343Glu
NM_001346091.1:c.705C>A	NP_001333020.1:p.Asp235Glu
NM_001346092.1:c.570C>A	NP_001333021.1:p.Asp190Glu
NR_144351.1:n.1258C>A
NM_001065.4:c.1029C>A MANE Select	NP_001056.1:p.Asp343Glu
NM_001346091.2:c.705C>A	NP_001333020.1:p.Asp235Glu
NM_001346092.2:c.570C>A	NP_001333021.1:p.Asp190Glu
NR_144351.2:n.1217C>A