Canonical Allele Identifier: CA383546922

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6439755C>A (hg19) ; chr12:g.6330589C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330589C>A , CM000674.2:g.6330589C>A	GRCh38
NC_000012.11:g.6439755C>A , CM000674.1:g.6439755C>A	GRCh37
NC_000012.10:g.6310016C>A	NCBI36
NG_007506.1:g.16507G>T , LRG_193:g.16507G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1840+9G>T
ENST00000437813.8:c.*200+9G>T	ENSP00000513672.1:n.*200+9G>T
ENST00000440083.7:c.958+9G>T	ENSP00000413224.3:n.958+9G>T
ENST00000535038.2:n.921+9G>T
ENST00000535958.2:c.*566+9G>T	ENSP00000513673.1:n.*566+9G>T
ENST00000698337.1:n.729+9G>T
ENST00000698338.1:n.1153+9G>T
ENST00000698339.1:c.*234+9G>T	ENSP00000513670.1:n.*234+9G>T
ENST00000698340.1:c.665+9G>T	ENSP00000513671.1:n.665+9G>T
ENST00000162749.7:c.739+9G>T MANE Select	ENSP00000162749.2:n.739+9G>T
ENST00000162749.6:c.739+9G>T	ENSP00000162749.2:n.739+9G>T
ENST00000534885.5:c.*216+9G>T	ENSP00000441803.1:n.*216+9G>T
ENST00000535038.1:n.550+9G>T
ENST00000536717.5:n.643+9G>T
ENST00000537842.5:n.343+9G>T
ENST00000539372.5:c.748G>T	ENSP00000442059.1:p.Gly250Trp
ENST00000540022.5:c.610+9G>T	ENSP00000438343.1:n.610+9G>T
ENST00000543359.5:n.151+9G>T
ENST00000543995.5:c.*326+9G>T	ENSP00000442405.1:n.*326+9G>T
NM_001065.3:c.739+9G>T , LRG_193t1:c.739+9G>T	NP_001056.1:n.739+9G>T
NM_001346091.1:c.415+9G>T	NP_001333020.1:n.415+9G>T
NM_001346092.1:c.280+9G>T	NP_001333021.1:n.280+9G>T
NR_144351.1:n.968+9G>T
NM_001065.4:c.739+9G>T MANE Select	NP_001056.1:n.739+9G>T
NM_001346091.2:c.415+9G>T	NP_001333020.1:n.415+9G>T
NM_001346092.2:c.280+9G>T	NP_001333021.1:n.280+9G>T
NR_144351.2:n.927+9G>T