Canonical Allele Identifier: CA504078208

Gene: TNFRSF11A

Linked Data

• MyVariant Identifiers: chr18:g.60025566C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.62358333C>G , CM000680.2:g.62358333C>G	GRCh38
NC_000018.9:g.60025566C>G , CM000680.1:g.60025566C>G	GRCh37
NC_000018.8:g.58176546C>G	NCBI36
NG_008098.1:g.38019C>G , LRG_194:g.38019C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000586569.3:c.513C>G MANE Select	ENSP00000465500.1:p.Pro171=
ENST00000639222.1:c.513C>G	ENSP00000492422.1:p.Pro171=
ENST00000269485.11:c.513C>G	ENSP00000269485.7:p.Pro171=
ENST00000586569.2:c.513C>G	ENSP00000465500.1:p.Pro171=
ENST00000587697.1:n.431C>G
ENST00000616710.4:c.513C>G	ENSP00000479567.1:p.Pro171=
ENST00000617039.4:c.513C>G	ENSP00000482466.1:p.Pro171=
NM_001270949.1:c.513C>G	NP_001257878.1:p.Pro171=
NM_001270950.1:c.513C>G	NP_001257879.1:p.Pro171=
NM_001270951.1:c.513C>G	NP_001257880.1:p.Pro171=
NM_001278268.1:c.471C>G	NP_001265197.1:p.Pro157=
NM_003839.3:c.513C>G	NP_003830.1:p.Pro171=
XM_011526244.1:c.528C>G	XP_011524546.1:p.Pro176=
XM_011526245.1:c.405C>G	XP_011524547.1:p.Pro135=
XR_935263.1:n.543C>G
XM_011526244.2:c.528C>G	XP_011524546.1:p.Pro176=
XM_011526245.2:c.405C>G	XP_011524547.1:p.Pro135=
XM_017026064.1:c.405C>G	XP_016881553.1:p.Pro135=
XM_017026065.1:c.363C>G	XP_016881554.1:p.Pro121=
XM_017026066.1:c.303C>G	XP_016881555.1:p.Pro101=
NM_003839.4:c.513C>G MANE Select	NP_003830.1:p.Pro171=
NM_001270951.2:c.513C>G	NP_001257880.1:p.Pro171=
NM_001278268.2:c.471C>G	NP_001265197.1:p.Pro157=
NM_001270949.2:c.513C>G	NP_001257878.1:p.Pro171=
NM_001270950.2:c.513C>G	NP_001257879.1:p.Pro171=