Canonical Allele Identifier: CA8983960

Gene: TNFRSF11A

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.62369314G>A , CM000680.2:g.62369314G>A	GRCh38
NC_000018.9:g.60036547G>A , CM000680.1:g.60036547G>A	GRCh37
NC_000018.8:g.58187527G>A	NCBI36
NG_008098.1:g.49000G>A , LRG_194:g.49000G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_003839.4:c.1397G>A MANE Select	NP_003830.1:p.Arg466His
ENST00000586569.3:c.1397G>A MANE Select	ENSP00000465500.1:p.Arg466His
NM_001270949.1:c.783+2554G>A	NP_001257878.1:n.783+2554G>A
NM_001270949.2:c.783+2554G>A	NP_001257878.1:n.783+2554G>A
NM_001270950.1:c.730+7521G>A	NP_001257879.1:n.730+7521G>A
NM_001270950.2:c.730+7521G>A	NP_001257879.1:n.730+7521G>A
NM_001270951.1:c.616+9265G>A	NP_001257880.1:n.616+9265G>A
NM_001270951.2:c.616+9265G>A	NP_001257880.1:n.616+9265G>A
NM_001278268.1:c.1355G>A	NP_001265197.1:p.Arg452His
NM_001278268.2:c.1355G>A	NP_001265197.1:p.Arg452His
NM_003839.3:c.1397G>A	NP_003830.1:p.Arg466His
ENST00000269485.11:c.616+9265G>A	ENSP00000269485.7:n.616+9265G>A
ENST00000586569.2:c.1397G>A	ENSP00000465500.1:p.Arg466His
ENST00000616710.4:c.783+2554G>A	ENSP00000479567.1:n.783+2554G>A
ENST00000617039.4:c.730+7521G>A	ENSP00000482466.1:n.730+7521G>A
XM_011526244.1:c.1412G>A	XP_011524546.1:p.Arg471His
XM_011526244.2:c.1412G>A	XP_011524546.1:p.Arg471His
XM_011526245.1:c.1289G>A	XP_011524547.1:p.Arg430His
XM_011526245.2:c.1289G>A	XP_011524547.1:p.Arg430His
XM_017026064.1:c.1289G>A	XP_016881553.1:p.Arg430His
XM_017026065.1:c.1247G>A	XP_016881554.1:p.Arg416His
XM_017026066.1:c.1187G>A	XP_016881555.1:p.Arg396His
XR_935263.1:n.1427G>A