Canonical Allele Identifier: CA483605019

Gene: TNFSF11

Linked Data

• ClinVar Variation Id: 793552
• ClinVar RCV Id: RCV000976737
• dbSNP Id: rs1594484298
• gnomAD v4: 13-42606570-C-T
• MyVariant Identifiers: chr13:g.43180706C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.42606570C>T , CM000675.2:g.42606570C>T	GRCh38
NC_000013.10:g.43180706C>T , CM000675.1:g.43180706C>T	GRCh37
NC_000013.9:g.42078706C>T	NCBI36
NG_008990.1:g.48835C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000398795.7:c.606C>T MANE Select	ENSP00000381775.3:p.Ser202=
ENST00000239849.8:c.465C>T	ENSP00000239849.7:p.Ser155=
ENST00000358545.6:c.387C>T	ENSP00000351347.2:p.Ser129=
ENST00000398795.6:c.606C>T	ENSP00000381775.3:p.Ser202=
ENST00000405262.6:c.387C>T	ENSP00000384042.2:p.Ser129=
ENST00000544862.5:c.387C>T	ENSP00000444913.1:p.Ser129=
NM_003701.3:c.606C>T	NP_003692.1:p.Ser202=
NM_033012.3:c.387C>T	NP_143026.1:p.Ser129=
XM_011535280.1:c.387C>T	XP_011533582.1:p.Ser129=
XM_011535280.2:c.387C>T	XP_011533582.1:p.Ser129=
XM_017020802.1:c.444C>T	XP_016876291.1:p.Ser148=
XM_017020803.2:c.387C>T	XP_016876292.1:p.Ser129=
NM_003701.4:c.606C>T MANE Select	NP_003692.1:p.Ser202=
NM_033012.4:c.387C>T	NP_143026.1:p.Ser129=