Canonical Allele Identifier: CA504078228

Gene: TNFRSF11A

Linked Data

• MyVariant Identifiers: chr18:g.60025572C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.62358339C>G , CM000680.2:g.62358339C>G	GRCh38
NC_000018.9:g.60025572C>G , CM000680.1:g.60025572C>G	GRCh37
NC_000018.8:g.58176552C>G	NCBI36
NG_008098.1:g.38025C>G , LRG_194:g.38025C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000586569.3:c.519C>G MANE Select	ENSP00000465500.1:p.Thr173=
ENST00000639222.1:c.519C>G	ENSP00000492422.1:p.Thr173=
ENST00000269485.11:c.519C>G	ENSP00000269485.7:p.Thr173=
ENST00000586569.2:c.519C>G	ENSP00000465500.1:p.Thr173=
ENST00000587697.1:n.437C>G
ENST00000616710.4:c.519C>G	ENSP00000479567.1:p.Thr173=
ENST00000617039.4:c.519C>G	ENSP00000482466.1:p.Thr173=
NM_001270949.1:c.519C>G	NP_001257878.1:p.Thr173=
NM_001270950.1:c.519C>G	NP_001257879.1:p.Thr173=
NM_001270951.1:c.519C>G	NP_001257880.1:p.Thr173=
NM_001278268.1:c.477C>G	NP_001265197.1:p.Thr159=
NM_003839.3:c.519C>G	NP_003830.1:p.Thr173=
XM_011526244.1:c.534C>G	XP_011524546.1:p.Thr178=
XM_011526245.1:c.411C>G	XP_011524547.1:p.Thr137=
XR_935263.1:n.549C>G
XM_011526244.2:c.534C>G	XP_011524546.1:p.Thr178=
XM_011526245.2:c.411C>G	XP_011524547.1:p.Thr137=
XM_017026064.1:c.411C>G	XP_016881553.1:p.Thr137=
XM_017026065.1:c.369C>G	XP_016881554.1:p.Thr123=
XM_017026066.1:c.309C>G	XP_016881555.1:p.Thr103=
NM_003839.4:c.519C>G MANE Select	NP_003830.1:p.Thr173=
NM_001270951.2:c.519C>G	NP_001257880.1:p.Thr173=
NM_001278268.2:c.477C>G	NP_001265197.1:p.Thr159=
NM_001270949.2:c.519C>G	NP_001257878.1:p.Thr173=
NM_001270950.2:c.519C>G	NP_001257879.1:p.Thr173=