Canonical Allele Identifier: CA14538800

Gene: TNFRSF11A

Linked Data

• ClinVar Variation Id: 1278941
• ClinVar RCV Id: RCV001690662
• dbSNP Id: rs8083511
• gnomAD v2: 18-60028655-A-C
• gnomAD v3: 18-62361422-A-C
• gnomAD v4: 18-62361422-A-C
• MyVariant Identifiers: chr18:g.60028655A>C (hg19) ; chr18:g.62361422A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.62361422A>C , CM000680.2:g.62361422A>C	GRCh38
NC_000018.9:g.60028655A>C , CM000680.1:g.60028655A>C	GRCh37
NC_000018.8:g.58179635A>C	NCBI36
NG_008098.1:g.41108A>C , LRG_194:g.41108A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000586569.3:c.617-258A>C MANE Select	ENSP00000465500.1:n.617-258A>C
ENST00000639222.1:c.617-258A>C	ENSP00000492422.1:n.617-258A>C
ENST00000269485.11:c.616+1373A>C	ENSP00000269485.7:n.616+1373A>C
ENST00000586569.2:c.617-258A>C	ENSP00000465500.1:n.617-258A>C
ENST00000616710.4:c.617-258A>C	ENSP00000479567.1:n.617-258A>C
ENST00000617039.4:c.617-258A>C	ENSP00000482466.1:n.617-258A>C
NM_001270949.1:c.617-258A>C	NP_001257878.1:n.617-258A>C
NM_001270950.1:c.617-258A>C	NP_001257879.1:n.617-258A>C
NM_001270951.1:c.616+1373A>C	NP_001257880.1:n.616+1373A>C
NM_001278268.1:c.575-258A>C	NP_001265197.1:n.575-258A>C
NM_003839.3:c.617-258A>C	NP_003830.1:n.617-258A>C
XM_011526244.1:c.632-258A>C	XP_011524546.1:n.632-258A>C
XM_011526245.1:c.509-258A>C	XP_011524547.1:n.509-258A>C
XR_935263.1:n.647-258A>C
XM_011526244.2:c.632-258A>C	XP_011524546.1:n.632-258A>C
XM_011526245.2:c.509-258A>C	XP_011524547.1:n.509-258A>C
XM_017026064.1:c.509-258A>C	XP_016881553.1:n.509-258A>C
XM_017026065.1:c.467-258A>C	XP_016881554.1:n.467-258A>C
XM_017026066.1:c.407-258A>C	XP_016881555.1:n.407-258A>C
NM_003839.4:c.617-258A>C MANE Select	NP_003830.1:n.617-258A>C
NM_001270951.2:c.616+1373A>C	NP_001257880.1:n.616+1373A>C
NM_001278268.2:c.575-258A>C	NP_001265197.1:n.575-258A>C
NM_001270949.2:c.617-258A>C	NP_001257878.1:n.617-258A>C
NM_001270950.2:c.617-258A>C	NP_001257879.1:n.617-258A>C