Canonical Allele Identifier: CA609696435

Gene: TNFSF11

Linked Data

• dbSNP Id: rs1220371696
• gnomAD v2: 13-43161000-G-A
• gnomAD v3: 13-42586864-G-A
• gnomAD v4: 13-42586864-G-A
• MyVariant Identifiers: chr13:g.43161000G>A (hg19) ; chr13:g.42586864G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.42586864G>A , CM000675.2:g.42586864G>A	GRCh38
NC_000013.10:g.43161000G>A , CM000675.1:g.43161000G>A	GRCh37
NC_000013.9:g.42059000G>A	NCBI36
NG_008990.1:g.29129G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000398795.7:c.387+5571G>A MANE Select	ENSP00000381775.3:n.387+5571G>A
ENST00000239849.8:c.246+5571G>A	ENSP00000239849.7:n.246+5571G>A
ENST00000358545.6:c.168+5571G>A	ENSP00000351347.2:n.168+5571G>A
ENST00000398795.6:c.387+5571G>A	ENSP00000381775.3:n.387+5571G>A
ENST00000405262.6:c.168+5571G>A	ENSP00000384042.2:n.168+5571G>A
ENST00000544862.5:c.168+5571G>A	ENSP00000444913.1:n.168+5571G>A
NM_003701.3:c.387+5571G>A	NP_003692.1:n.387+5571G>A
NM_033012.3:c.168+5571G>A	NP_143026.1:n.168+5571G>A
XM_011535280.1:c.168+5571G>A	XP_011533582.1:n.168+5571G>A
XM_011535280.2:c.168+5571G>A	XP_011533582.1:n.168+5571G>A
XM_017020802.1:c.225+5571G>A	XP_016876291.1:n.225+5571G>A
XM_017020803.2:c.168+5571G>A	XP_016876292.1:n.168+5571G>A
NM_003701.4:c.387+5571G>A MANE Select	NP_003692.1:n.387+5571G>A
NM_033012.4:c.168+5571G>A	NP_143026.1:n.168+5571G>A