Canonical Allele Identifier: CA10648062

Gene: TNFRSF11A

Linked Data

• ClinVar Variation Id: 327754
• ClinVar RCV Id: RCV000312407 ; RCV000400565
• dbSNP Id: rs886054096
• gnomAD v2: 18-60052972-G-A
• gnomAD v3: 18-62385739-G-A
• gnomAD v4: 18-62385739-G-A
• MyVariant Identifiers: chr18:g.60052972G>A (hg19) ; chr18:g.62385739G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.62385739G>A , CM000680.2:g.62385739G>A	GRCh38
NC_000018.9:g.60052972G>A , CM000680.1:g.60052972G>A	GRCh37
NC_000018.8:g.58203952G>A	NCBI36
NG_008098.1:g.65425G>A , LRG_194:g.65425G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000586569.3:c.*705G>A MANE Select	ENSP00000465500.1:n.*705G>A
ENST00000269485.11:c.*705G>A	ENSP00000269485.7:n.*705G>A
ENST00000586569.2:c.*705G>A	ENSP00000465500.1:n.*705G>A
ENST00000616710.4:c.*980G>A	ENSP00000479567.1:n.*980G>A
ENST00000617039.4:c.*705G>A	ENSP00000482466.1:n.*705G>A
NM_001270949.1:c.*980G>A	NP_001257878.1:n.*980G>A
NM_001270950.1:c.*705G>A	NP_001257879.1:n.*705G>A
NM_001270951.1:c.*705G>A	NP_001257880.1:n.*705G>A
NM_001278268.1:c.*705G>A	NP_001265197.1:n.*705G>A
NM_003839.3:c.*705G>A	NP_003830.1:n.*705G>A
XM_011526244.2:c.*705G>A	XP_011524546.1:n.*705G>A
XM_011526245.2:c.*705G>A	XP_011524547.1:n.*705G>A
XM_017026064.1:c.*705G>A	XP_016881553.1:n.*705G>A
XM_017026065.1:c.*705G>A	XP_016881554.1:n.*705G>A
XM_017026066.1:c.*705G>A	XP_016881555.1:n.*705G>A
NM_003839.4:c.*705G>A MANE Select	NP_003830.1:n.*705G>A
NM_001270951.2:c.*705G>A	NP_001257880.1:n.*705G>A
NM_001278268.2:c.*705G>A	NP_001265197.1:n.*705G>A
NM_001270949.2:c.*980G>A	NP_001257878.1:n.*980G>A
NM_001270950.2:c.*705G>A	NP_001257879.1:n.*705G>A