Canonical Allele Identifier: CA8983715

Gene: TNFRSF11A

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.62354509G>A , CM000680.2:g.62354509G>A	GRCh38
NC_000018.9:g.60021742G>A , CM000680.1:g.60021742G>A	GRCh37
NC_000018.8:g.58172722G>A	NCBI36
NG_008098.1:g.34195G>A , LRG_194:g.34195G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_003839.4:c.402G>A MANE Select	NP_003830.1:p.Ala134=
ENST00000586569.3:c.402G>A MANE Select	ENSP00000465500.1:p.Ala134=
NM_001270949.1:c.402G>A	NP_001257878.1:p.Ala134=
NM_001270949.2:c.402G>A	NP_001257878.1:p.Ala134=
NM_001270950.1:c.402G>A	NP_001257879.1:p.Ala134=
NM_001270950.2:c.402G>A	NP_001257879.1:p.Ala134=
NM_001270951.1:c.402G>A	NP_001257880.1:p.Ala134=
NM_001270951.2:c.402G>A	NP_001257880.1:p.Ala134=
NM_001278268.1:c.402G>A	NP_001265197.1:p.Ala134=
NM_001278268.2:c.402G>A	NP_001265197.1:p.Ala134=
NM_003839.3:c.402G>A	NP_003830.1:p.Ala134=
ENST00000269485.11:c.402G>A	ENSP00000269485.7:p.Ala134=
ENST00000586569.2:c.402G>A	ENSP00000465500.1:p.Ala134=
ENST00000616710.4:c.402G>A	ENSP00000479567.1:p.Ala134=
ENST00000617039.4:c.402G>A	ENSP00000482466.1:p.Ala134=
ENST00000639222.1:c.402G>A	ENSP00000492422.1:p.Ala134=
XM_011526244.1:c.402G>A	XP_011524546.1:p.Ala134=
XM_011526244.2:c.402G>A	XP_011524546.1:p.Ala134=
XM_011526245.1:c.284G>A	XP_011524547.1:p.Arg95His
XM_011526245.2:c.284G>A	XP_011524547.1:p.Arg95His
XM_017026064.1:c.284G>A	XP_016881553.1:p.Arg95His
XM_017026065.1:c.237G>A	XP_016881554.1:p.Ala79=
XM_017026066.1:c.182G>A	XP_016881555.1:p.Arg61His
XR_935263.1:n.417G>A