Canonical Allele Identifier: CA504079034

Gene: TNFRSF11A

Linked Data

• MyVariant Identifiers: chr18:g.60027230G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.62359997G>A , CM000680.2:g.62359997G>A	GRCh38
NC_000018.9:g.60027230G>A , CM000680.1:g.60027230G>A	GRCh37
NC_000018.8:g.58178210G>A	NCBI36
NG_008098.1:g.39683G>A , LRG_194:g.39683G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000586569.3:c.564G>A MANE Select	ENSP00000465500.1:p.Glu188=
ENST00000639222.1:c.564G>A	ENSP00000492422.1:p.Glu188=
ENST00000269485.11:c.564G>A	ENSP00000269485.7:p.Glu188=
ENST00000586569.2:c.564G>A	ENSP00000465500.1:p.Glu188=
ENST00000587697.1:n.482G>A
ENST00000616710.4:c.564G>A	ENSP00000479567.1:p.Glu188=
ENST00000617039.4:c.564G>A	ENSP00000482466.1:p.Glu188=
NM_001270949.1:c.564G>A	NP_001257878.1:p.Glu188=
NM_001270950.1:c.564G>A	NP_001257879.1:p.Glu188=
NM_001270951.1:c.564G>A	NP_001257880.1:p.Glu188=
NM_001278268.1:c.522G>A	NP_001265197.1:p.Glu174=
NM_003839.3:c.564G>A	NP_003830.1:p.Glu188=
XM_011526244.1:c.579G>A	XP_011524546.1:p.Glu193=
XM_011526245.1:c.456G>A	XP_011524547.1:p.Glu152=
XR_935263.1:n.594G>A
XM_011526244.2:c.579G>A	XP_011524546.1:p.Glu193=
XM_011526245.2:c.456G>A	XP_011524547.1:p.Glu152=
XM_017026064.1:c.456G>A	XP_016881553.1:p.Glu152=
XM_017026065.1:c.414G>A	XP_016881554.1:p.Glu138=
XM_017026066.1:c.354G>A	XP_016881555.1:p.Glu118=
NM_003839.4:c.564G>A MANE Select	NP_003830.1:p.Glu188=
NM_001270951.2:c.564G>A	NP_001257880.1:p.Glu188=
NM_001278268.2:c.522G>A	NP_001265197.1:p.Glu174=
NM_001270949.2:c.564G>A	NP_001257878.1:p.Glu188=
NM_001270950.2:c.564G>A	NP_001257879.1:p.Glu188=