Canonical Allele Identifier: CA402613410

Gene: TNFRSF11A

Linked Data

• MyVariant Identifiers: chr18:g.60025562G>C (hg19) ; chr18:g.62358329G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.62358329G>C , CM000680.2:g.62358329G>C	GRCh38
NC_000018.9:g.60025562G>C , CM000680.1:g.60025562G>C	GRCh37
NC_000018.8:g.58176542G>C	NCBI36
NG_008098.1:g.38015G>C , LRG_194:g.38015G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000586569.3:c.509G>C MANE Select	ENSP00000465500.1:p.Arg170Thr
ENST00000639222.1:c.509G>C	ENSP00000492422.1:p.Arg170Thr
ENST00000269485.11:c.509G>C	ENSP00000269485.7:p.Arg170Thr
ENST00000586569.2:c.509G>C	ENSP00000465500.1:p.Arg170Thr
ENST00000587697.1:n.427G>C
ENST00000616710.4:c.509G>C	ENSP00000479567.1:p.Arg170Thr
ENST00000617039.4:c.509G>C	ENSP00000482466.1:p.Arg170Thr
NM_001270949.1:c.509G>C	NP_001257878.1:p.Arg170Thr
NM_001270950.1:c.509G>C	NP_001257879.1:p.Arg170Thr
NM_001270951.1:c.509G>C	NP_001257880.1:p.Arg170Thr
NM_001278268.1:c.467G>C	NP_001265197.1:p.Arg156Thr
NM_003839.3:c.509G>C	NP_003830.1:p.Arg170Thr
XM_011526244.1:c.524G>C	XP_011524546.1:p.Arg175Thr
XM_011526245.1:c.401G>C	XP_011524547.1:p.Arg134Thr
XR_935263.1:n.539G>C
XM_011526244.2:c.524G>C	XP_011524546.1:p.Arg175Thr
XM_011526245.2:c.401G>C	XP_011524547.1:p.Arg134Thr
XM_017026064.1:c.401G>C	XP_016881553.1:p.Arg134Thr
XM_017026065.1:c.359G>C	XP_016881554.1:p.Arg120Thr
XM_017026066.1:c.299G>C	XP_016881555.1:p.Arg100Thr
NM_003839.4:c.509G>C MANE Select	NP_003830.1:p.Arg170Thr
NM_001270951.2:c.509G>C	NP_001257880.1:p.Arg170Thr
NM_001278268.2:c.467G>C	NP_001265197.1:p.Arg156Thr
NM_001270949.2:c.509G>C	NP_001257878.1:p.Arg170Thr
NM_001270950.2:c.509G>C	NP_001257879.1:p.Arg170Thr