Canonical Allele Identifier: CA201625

Gene: TNFSF11

Linked Data

• ClinVar Variation Id: 195202
• ClinVar RCV Id: RCV000175758 ; RCV000400844 ; RCV001511770
• dbSNP Id: rs2277439
• ExAC: 13:43155443 G / A
• gnomAD v2: 13-43155443-G-A
• gnomAD v3: 13-42581307-G-A
• gnomAD v4: 13-42581307-G-A
• MyVariant Identifiers: chr13:g.43155443G>A (hg19) ; chr13:g.42581307G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.42581307G>A , CM000675.2:g.42581307G>A	GRCh38
NC_000013.10:g.43155443G>A , CM000675.1:g.43155443G>A	GRCh37
NC_000013.9:g.42053443G>A	NCBI36
NG_008990.1:g.23572G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398795.7:c.387+14G>A MANE Select	ENSP00000381775.3:n.387+14G>A
ENST00000239849.8:c.246+14G>A	ENSP00000239849.7:n.246+14G>A
ENST00000358545.6:c.168+14G>A	ENSP00000351347.2:n.168+14G>A
ENST00000398795.6:c.387+14G>A	ENSP00000381775.3:n.387+14G>A
ENST00000405262.6:c.168+14G>A	ENSP00000384042.2:n.168+14G>A
ENST00000544862.5:c.168+14G>A	ENSP00000444913.1:n.168+14G>A
NM_003701.3:c.387+14G>A	NP_003692.1:n.387+14G>A
NM_033012.3:c.168+14G>A	NP_143026.1:n.168+14G>A
XM_011535280.1:c.168+14G>A	XP_011533582.1:n.168+14G>A
XM_011535280.2:c.168+14G>A	XP_011533582.1:n.168+14G>A
XM_017020802.1:c.225+14G>A	XP_016876291.1:n.225+14G>A
XM_017020803.2:c.168+14G>A	XP_016876292.1:n.168+14G>A
NM_003701.4:c.387+14G>A MANE Select	NP_003692.1:n.387+14G>A
NM_033012.4:c.168+14G>A	NP_143026.1:n.168+14G>A