Canonical Allele Identifier: CA2739272242

Gene: TNFRSF9

Linked Data

• ClinVar Variation Id: 2790765
• ClinVar RCV Id: RCV003670075

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.7937711_7937712delinsAT , CM000663.2:g.7937711_7937712delinsAT	GRCh38
NC_000001.10:g.7997771_7997772delinsAT , CM000663.1:g.7997771_7997772delinsAT	GRCh37
NC_000001.9:g.7920358_7920359delinsAT	NCBI36
NG_052834.1:g.10454_10455delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377507.8:c.391_392delinsAT MANE Select	ENSP00000366729.3:p.Gly131Ile
ENST00000377507.7:c.391_392delinsAT	ENSP00000366729.3:p.Gly131Ile
ENST00000492571.1:c.157_158delinsAT	ENSP00000464978.1:p.Gly53Ile
ENST00000615230.4:c.391_392delinsAT	ENSP00000478699.1:p.Gly131Ile
NM_001561.5:c.391_392delinsAT	NP_001552.2:p.Gly131Ile
XM_006710618.2:c.391_392delinsAT	XP_006710681.1:p.Gly131Ile
XM_011541386.1:c.391_392delinsAT	XP_011539688.1:p.Gly131Ile
XM_006710618.3:c.391_392delinsAT	XP_006710681.1:p.Gly131Ile
XM_011541386.2:c.391_392delinsAT	XP_011539688.1:p.Gly131Ile
NM_001561.6:c.391_392delinsAT MANE Select	NP_001552.2:p.Gly131Ile