Canonical Allele Identifier: CA383550304

Gene: TNFRSF1A

Linked Data

• gnomAD v4: 12-6333505-C-A
• MyVariant Identifiers: chr12:g.6442671C>A (hg19) ; chr12:g.6333505C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6333505C>A , CM000674.2:g.6333505C>A	GRCh38
NC_000012.11:g.6442671C>A , CM000674.1:g.6442671C>A	GRCh37
NC_000012.10:g.6312932C>A	NCBI36
NG_007506.1:g.13591G>T , LRG_193:g.13591G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.368G>T
ENST00000437813.8:c.334G>T	ENSP00000513672.1:p.Val112Leu
ENST00000440083.7:c.334G>T	ENSP00000413224.3:p.Val112Leu
ENST00000535958.2:c.*161G>T	ENSP00000513673.1:n.*161G>T
ENST00000698339.1:c.334G>T	ENSP00000513670.1:p.Val112Leu
ENST00000698340.1:c.334G>T	ENSP00000513671.1:p.Val112Leu
ENST00000162749.7:c.334G>T MANE Select	ENSP00000162749.2:p.Val112Leu
ENST00000162749.6:c.334G>T	ENSP00000162749.2:p.Val112Leu
ENST00000366159.8:c.334G>T	ENSP00000380389.3:p.Val112Leu
ENST00000437813.7:n.295G>T
ENST00000440083.6:c.334G>T	ENSP00000413224.2:p.Val112Leu
ENST00000534885.5:c.180G>T	ENSP00000441803.1:p.Arg60Ser
ENST00000536194.1:c.307G>T	ENSP00000442919.1:p.Val103Leu
ENST00000539372.5:c.334G>T	ENSP00000442059.1:p.Val112Leu
ENST00000540022.5:c.205G>T	ENSP00000438343.1:p.Val69Leu
ENST00000543048.5:c.215-54G>T	ENSP00000439981.1:n.215-54G>T
ENST00000543995.5:c.194-54G>T	ENSP00000442405.1:n.194-54G>T
NM_001065.3:c.334G>T , LRG_193t1:c.334G>T	NP_001056.1:p.Val112Leu
NM_001346091.1:c.10G>T	NP_001333020.1:p.Val4Leu
NM_001346092.1:c.-244G>T	NP_001333021.1:n.-244G>T
NR_144351.1:n.637G>T
NM_001065.4:c.334G>T MANE Select	NP_001056.1:p.Val112Leu
NM_001346091.2:c.10G>T	NP_001333020.1:p.Val4Leu
NM_001346092.2:c.-244G>T	NP_001333021.1:n.-244G>T
NR_144351.2:n.596G>T