Canonical Allele Identifier: CA8350899

Gene: TNFSF12 TNFSF12-TNFSF13

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7557274G>A , CM000679.2:g.7557274G>A	GRCh38
NC_000017.10:g.7460591G>A , CM000679.1:g.7460591G>A	GRCh37
NC_000017.9:g.7401315G>A	NCBI36
NG_029949.1:g.3983G>A
NG_052944.1:g.13217G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_003809.3:c.674G>A (TNFSF12) MANE Select	NP_003800.1:p.Arg225Gln
ENST00000293825.11:c.674G>A (TNFSF12) MANE Select	ENSP00000293825.6:p.Arg225Gln
NM_003809.2:c.674G>A (TNFSF12)	NP_003800.1:p.Arg225Gln
NM_172089.3:c.498+372G>A (TNFSF12-TNFSF13)	NP_742086.1:n.498+372G>A
NM_172089.4:c.498+372G>A (TNFSF12-TNFSF13)	NP_742086.1:n.498+372G>A
NR_037146.1:n.1009G>A (TNFSF12)
NR_037146.2:n.1009G>A (TNFSF12)
ENST00000293825.10:c.674G>A (TNFSF12)	ENSP00000293825.6:p.Arg225Gln
ENST00000293826.4:c.498+372G>A (TNFSF12-TNFSF13)	ENSP00000293826.4:n.498+372G>A
ENST00000322272.11:c.*508G>A (TNFSF12)	ENSP00000314636.7:n.*508G>A
ENST00000462619.6:n.791G>A (TNFSF12)
ENST00000462811.1:n.505G>A (TNFSF12)
ENST00000462811.2:n.512G>A (TNFSF12)
ENST00000700015.1:c.677G>A (TNFSF12)	ENSP00000514756.1:p.Arg226Gln
ENST00000700047.1:n.676G>A (TNFSF12)
ENST00000700048.1:n.918G>A (TNFSF12)
ENST00000700049.1:n.670G>A (TNFSF12)
ENST00000700050.1:n.921G>A (TNFSF12)
ENST00000700052.1:c.*165G>A (TNFSF12)	ENSP00000514764.1:n.*165G>A
ENST00000700053.1:c.671G>A (TNFSF12)	ENSP00000514765.1:p.Arg224Gln
ENST00000700054.1:c.*384G>A (TNFSF12)	ENSP00000514766.1:n.*384G>A
ENST00000700056.1:c.*508G>A (TNFSF12)	ENSP00000514767.1:n.*508G>A
ENST00000700058.1:n.776G>A (TNFSF12)
ENST00000700059.1:n.1043G>A (TNFSF12)