Canonical Allele Identifier: CA10648056

Gene: TNFRSF11A

Linked Data

• ClinVar Variation Id: 327725
• ClinVar RCV Id: RCV000283697 ; RCV000341445 ; RCV003765898
• dbSNP Id: rs886054083
• gnomAD v4: 18-62325420-G-A
• MyVariant Identifiers: chr18:g.59992653G>A (hg19) ; chr18:g.62325420G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.62325420G>A , CM000680.2:g.62325420G>A	GRCh38
NC_000018.9:g.59992653G>A , CM000680.1:g.59992653G>A	GRCh37
NC_000018.8:g.58143633G>A	NCBI36
NG_008098.1:g.5106G>A , LRG_194:g.5106G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000586569.3:c.68G>A MANE Select	ENSP00000465500.1:p.Arg23Gln
ENST00000639222.1:c.68G>A	ENSP00000492422.1:p.Arg23Gln
ENST00000269485.11:c.68G>A	ENSP00000269485.7:p.Arg23Gln
ENST00000586569.2:c.68G>A	ENSP00000465500.1:p.Arg23Gln
ENST00000592013.1:n.95G>A
ENST00000616710.4:c.68G>A	ENSP00000479567.1:p.Arg23Gln
ENST00000617039.4:c.68G>A	ENSP00000482466.1:p.Arg23Gln
NM_001270949.1:c.68G>A	NP_001257878.1:p.Arg23Gln
NM_001270950.1:c.68G>A	NP_001257879.1:p.Arg23Gln
NM_001270951.1:c.68G>A	NP_001257880.1:p.Arg23Gln
NM_001278268.1:c.68G>A	NP_001265197.1:p.Arg23Gln
NM_003839.3:c.68G>A	NP_003830.1:p.Arg23Gln
XM_011526244.1:c.68G>A	XP_011524546.1:p.Arg23Gln
XM_011526245.1:c.-125G>A	XP_011524547.1:n.-125G>A
XR_935263.1:n.83G>A
XM_011526244.2:c.68G>A	XP_011524546.1:p.Arg23Gln
XM_011526245.2:c.-125G>A	XP_011524547.1:n.-125G>A
NM_003839.4:c.68G>A MANE Select	NP_003830.1:p.Arg23Gln
NM_001270951.2:c.68G>A	NP_001257880.1:p.Arg23Gln
NM_001278268.2:c.68G>A	NP_001265197.1:p.Arg23Gln
NM_001270949.2:c.68G>A	NP_001257878.1:p.Arg23Gln
NM_001270950.2:c.68G>A	NP_001257879.1:p.Arg23Gln