Canonical Allele Identifier: CA609696436

Gene: TNFSF11

Linked Data

• dbSNP Id: rs1258541441
• gnomAD v2: 13-43161006-T-TAA
• gnomAD v3: 13-42586870-T-TAA
• gnomAD v4: 13-42586870-T-TAA
• MyVariant Identifiers: chr13:g.43161006_43161007insAA (hg19) ; chr13:g.42586870_42586871insAA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.42586871_42586872insAA , CM000675.2:g.42586871_42586872insAA	GRCh38
NC_000013.10:g.43161007_43161008insAA , CM000675.1:g.43161007_43161008insAA	GRCh37
NC_000013.9:g.42059007_42059008insAA	NCBI36
NG_008990.1:g.29136_29137insAA

Transcript Alleles

HGVS	Amino-acid change
ENST00000398795.7:c.387+5578_387+5579insAA MANE Select	ENSP00000381775.3:n.387+5578_387+5579insAA
ENST00000239849.8:c.246+5578_246+5579insAA	ENSP00000239849.7:n.246+5578_246+5579insAA
ENST00000358545.6:c.168+5578_168+5579insAA	ENSP00000351347.2:n.168+5578_168+5579insAA
ENST00000398795.6:c.387+5578_387+5579insAA	ENSP00000381775.3:n.387+5578_387+5579insAA
ENST00000405262.6:c.168+5578_168+5579insAA	ENSP00000384042.2:n.168+5578_168+5579insAA
ENST00000544862.5:c.168+5578_168+5579insAA	ENSP00000444913.1:n.168+5578_168+5579insAA
NM_003701.3:c.387+5578_387+5579insAA	NP_003692.1:n.387+5578_387+5579insAA
NM_033012.3:c.168+5578_168+5579insAA	NP_143026.1:n.168+5578_168+5579insAA
XM_011535280.1:c.168+5578_168+5579insAA	XP_011533582.1:n.168+5578_168+5579insAA
XM_011535280.2:c.168+5578_168+5579insAA	XP_011533582.1:n.168+5578_168+5579insAA
XM_017020802.1:c.225+5578_225+5579insAA	XP_016876291.1:n.225+5578_225+5579insAA
XM_017020803.2:c.168+5578_168+5579insAA	XP_016876292.1:n.168+5578_168+5579insAA
NM_003701.4:c.387+5578_387+5579insAA MANE Select	NP_003692.1:n.387+5578_387+5579insAA
NM_033012.4:c.168+5578_168+5579insAA	NP_143026.1:n.168+5578_168+5579insAA