Canonical Allele Identifier: CA8983649

Gene: TNFRSF11A

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.62348225C>T , CM000680.2:g.62348225C>T	GRCh38
NC_000018.9:g.60015458C>T , CM000680.1:g.60015458C>T	GRCh37
NC_000018.8:g.58166438C>T	NCBI36
NG_008098.1:g.27911C>T , LRG_194:g.27911C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_003839.4:c.133C>T MANE Select	NP_003830.1:p.Arg45Trp
ENST00000586569.3:c.133C>T MANE Select	ENSP00000465500.1:p.Arg45Trp
NM_001270949.1:c.133C>T	NP_001257878.1:p.Arg45Trp
NM_001270949.2:c.133C>T	NP_001257878.1:p.Arg45Trp
NM_001270950.1:c.133C>T	NP_001257879.1:p.Arg45Trp
NM_001270950.2:c.133C>T	NP_001257879.1:p.Arg45Trp
NM_001270951.1:c.133C>T	NP_001257880.1:p.Arg45Trp
NM_001270951.2:c.133C>T	NP_001257880.1:p.Arg45Trp
NM_001278268.1:c.133C>T	NP_001265197.1:p.Arg45Trp
NM_001278268.2:c.133C>T	NP_001265197.1:p.Arg45Trp
NM_003839.3:c.133C>T	NP_003830.1:p.Arg45Trp
ENST00000269485.11:c.133C>T	ENSP00000269485.7:p.Arg45Trp
ENST00000586569.2:c.133C>T	ENSP00000465500.1:p.Arg45Trp
ENST00000616710.4:c.133C>T	ENSP00000479567.1:p.Arg45Trp
ENST00000617039.4:c.133C>T	ENSP00000482466.1:p.Arg45Trp
ENST00000639222.1:c.133C>T	ENSP00000492422.1:p.Arg45Trp
XM_011526244.1:c.133C>T	XP_011524546.1:p.Arg45Trp
XM_011526244.2:c.133C>T	XP_011524546.1:p.Arg45Trp
XM_011526245.1:c.15C>T	XP_011524547.1:p.Asp5=
XM_011526245.2:c.15C>T	XP_011524547.1:p.Asp5=
XM_017026064.1:c.15C>T	XP_016881553.1:p.Asp5=
XM_017026065.1:c.-158C>T	XP_016881554.1:n.-158C>T
XM_017026066.1:c.-213C>T	XP_016881555.1:n.-213C>T
XR_935263.1:n.148C>T