Canonical Allele Identifier: CA504079095

Gene: TNFRSF11A

Linked Data

• ClinVar Variation Id: 1945267
• ClinVar RCV Id: RCV002667096
• dbSNP Id: rs1157796855
• gnomAD v2: 18-60027248-C-T
• gnomAD v3: 18-62360015-C-T
• gnomAD v4: 18-62360015-C-T
• MyVariant Identifiers: chr18:g.60027248C>T (hg19) ; chr18:g.62360015C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.62360015C>T , CM000680.2:g.62360015C>T	GRCh38
NC_000018.9:g.60027248C>T , CM000680.1:g.60027248C>T	GRCh37
NC_000018.8:g.58178228C>T	NCBI36
NG_008098.1:g.39701C>T , LRG_194:g.39701C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000586569.3:c.582C>T MANE Select	ENSP00000465500.1:p.Cys194=
ENST00000639222.1:c.582C>T	ENSP00000492422.1:p.Cys194=
ENST00000269485.11:c.582C>T	ENSP00000269485.7:p.Cys194=
ENST00000586569.2:c.582C>T	ENSP00000465500.1:p.Cys194=
ENST00000587697.1:n.500C>T
ENST00000616710.4:c.582C>T	ENSP00000479567.1:p.Cys194=
ENST00000617039.4:c.582C>T	ENSP00000482466.1:p.Cys194=
NM_001270949.1:c.582C>T	NP_001257878.1:p.Cys194=
NM_001270950.1:c.582C>T	NP_001257879.1:p.Cys194=
NM_001270951.1:c.582C>T	NP_001257880.1:p.Cys194=
NM_001278268.1:c.540C>T	NP_001265197.1:p.Cys180=
NM_003839.3:c.582C>T	NP_003830.1:p.Cys194=
XM_011526244.1:c.597C>T	XP_011524546.1:p.Cys199=
XM_011526245.1:c.474C>T	XP_011524547.1:p.Cys158=
XR_935263.1:n.612C>T
XM_011526244.2:c.597C>T	XP_011524546.1:p.Cys199=
XM_011526245.2:c.474C>T	XP_011524547.1:p.Cys158=
XM_017026064.1:c.474C>T	XP_016881553.1:p.Cys158=
XM_017026065.1:c.432C>T	XP_016881554.1:p.Cys144=
XM_017026066.1:c.372C>T	XP_016881555.1:p.Cys124=
NM_003839.4:c.582C>T MANE Select	NP_003830.1:p.Cys194=
NM_001270951.2:c.582C>T	NP_001257880.1:p.Cys194=
NM_001278268.2:c.540C>T	NP_001265197.1:p.Cys180=
NM_001270949.2:c.582C>T	NP_001257878.1:p.Cys194=
NM_001270950.2:c.582C>T	NP_001257879.1:p.Cys194=