Canonical Allele Identifier: CA402613456

Gene: TNFRSF11A

Linked Data

• MyVariant Identifiers: chr18:g.60025569G>C (hg19) ; chr18:g.62358336G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.62358336G>C , CM000680.2:g.62358336G>C	GRCh38
NC_000018.9:g.60025569G>C , CM000680.1:g.60025569G>C	GRCh37
NC_000018.8:g.58176549G>C	NCBI36
NG_008098.1:g.38022G>C , LRG_194:g.38022G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000586569.3:c.516G>C MANE Select	ENSP00000465500.1:p.Trp172Cys
ENST00000639222.1:c.516G>C	ENSP00000492422.1:p.Trp172Cys
ENST00000269485.11:c.516G>C	ENSP00000269485.7:p.Trp172Cys
ENST00000586569.2:c.516G>C	ENSP00000465500.1:p.Trp172Cys
ENST00000587697.1:n.434G>C
ENST00000616710.4:c.516G>C	ENSP00000479567.1:p.Trp172Cys
ENST00000617039.4:c.516G>C	ENSP00000482466.1:p.Trp172Cys
NM_001270949.1:c.516G>C	NP_001257878.1:p.Trp172Cys
NM_001270950.1:c.516G>C	NP_001257879.1:p.Trp172Cys
NM_001270951.1:c.516G>C	NP_001257880.1:p.Trp172Cys
NM_001278268.1:c.474G>C	NP_001265197.1:p.Trp158Cys
NM_003839.3:c.516G>C	NP_003830.1:p.Trp172Cys
XM_011526244.1:c.531G>C	XP_011524546.1:p.Trp177Cys
XM_011526245.1:c.408G>C	XP_011524547.1:p.Trp136Cys
XR_935263.1:n.546G>C
XM_011526244.2:c.531G>C	XP_011524546.1:p.Trp177Cys
XM_011526245.2:c.408G>C	XP_011524547.1:p.Trp136Cys
XM_017026064.1:c.408G>C	XP_016881553.1:p.Trp136Cys
XM_017026065.1:c.366G>C	XP_016881554.1:p.Trp122Cys
XM_017026066.1:c.306G>C	XP_016881555.1:p.Trp102Cys
NM_003839.4:c.516G>C MANE Select	NP_003830.1:p.Trp172Cys
NM_001270951.2:c.516G>C	NP_001257880.1:p.Trp172Cys
NM_001278268.2:c.474G>C	NP_001265197.1:p.Trp158Cys
NM_001270949.2:c.516G>C	NP_001257878.1:p.Trp172Cys
NM_001270950.2:c.516G>C	NP_001257879.1:p.Trp172Cys