Canonical Allele Identifier: CA2308284534

Gene: TNFRSF11A

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.62358328A= , CM000680.2:g.62358328A=	GRCh38
NC_000018.9:g.60025561A= , CM000680.1:g.60025561A=	GRCh37
NC_000018.8:g.58176541A=	NCBI36
NG_008098.1:g.38014A= , LRG_194:g.38014A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000586569.3:c.508A= MANE Select	ENSP00000465500.1:p.Arg170=
ENST00000639222.1:c.508A=	ENSP00000492422.1:p.Arg170=
ENST00000269485.11:c.508A=	ENSP00000269485.7:p.Arg170=
ENST00000586569.2:c.508A=	ENSP00000465500.1:p.Arg170=
ENST00000587697.1:n.426A=
ENST00000616710.4:c.508A=	ENSP00000479567.1:p.Arg170=
ENST00000617039.4:c.508A=	ENSP00000482466.1:p.Arg170=
NM_001270949.1:c.508A=	NP_001257878.1:p.Arg170=
NM_001270950.1:c.508A=	NP_001257879.1:p.Arg170=
NM_001270951.1:c.508A=	NP_001257880.1:p.Arg170=
NM_001278268.1:c.466A=	NP_001265197.1:p.Arg156=
NM_003839.3:c.508A=	NP_003830.1:p.Arg170=
XM_011526244.1:c.523A=	XP_011524546.1:p.Arg175=
XM_011526245.1:c.400A=	XP_011524547.1:p.Arg134=
XR_935263.1:n.538A=
XM_011526244.2:c.523A=	XP_011524546.1:p.Arg175=
XM_011526245.2:c.400A=	XP_011524547.1:p.Arg134=
XM_017026064.1:c.400A=	XP_016881553.1:p.Arg134=
XM_017026065.1:c.358A=	XP_016881554.1:p.Arg120=
XM_017026066.1:c.298A=	XP_016881555.1:p.Arg100=
NM_003839.4:c.508A= MANE Select	NP_003830.1:p.Arg170=
NM_001270951.2:c.508A=	NP_001257880.1:p.Arg170=
NM_001278268.2:c.466A=	NP_001265197.1:p.Arg156=
NM_001270949.2:c.508A=	NP_001257878.1:p.Arg170=
NM_001270950.2:c.508A=	NP_001257879.1:p.Arg170=