Canonical Allele Identifier: CA8983907

Gene: TNFRSF11A

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.62368935T>A , CM000680.2:g.62368935T>A	GRCh38
NC_000018.9:g.60036168T>A , CM000680.1:g.60036168T>A	GRCh37
NC_000018.8:g.58187148T>A	NCBI36
NG_008098.1:g.48621T>A , LRG_194:g.48621T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_003839.4:c.1018T>A MANE Select	NP_003830.1:p.Phe340Ile
ENST00000586569.3:c.1018T>A MANE Select	ENSP00000465500.1:p.Phe340Ile
NM_001270949.1:c.783+2175T>A	NP_001257878.1:n.783+2175T>A
NM_001270949.2:c.783+2175T>A	NP_001257878.1:n.783+2175T>A
NM_001270950.1:c.730+7142T>A	NP_001257879.1:n.730+7142T>A
NM_001270950.2:c.730+7142T>A	NP_001257879.1:n.730+7142T>A
NM_001270951.1:c.616+8886T>A	NP_001257880.1:n.616+8886T>A
NM_001270951.2:c.616+8886T>A	NP_001257880.1:n.616+8886T>A
NM_001278268.1:c.976T>A	NP_001265197.1:p.Phe326Ile
NM_001278268.2:c.976T>A	NP_001265197.1:p.Phe326Ile
NM_003839.3:c.1018T>A	NP_003830.1:p.Phe340Ile
ENST00000269485.11:c.616+8886T>A	ENSP00000269485.7:n.616+8886T>A
ENST00000586569.2:c.1018T>A	ENSP00000465500.1:p.Phe340Ile
ENST00000616710.4:c.783+2175T>A	ENSP00000479567.1:n.783+2175T>A
ENST00000617039.4:c.730+7142T>A	ENSP00000482466.1:n.730+7142T>A
XM_011526244.1:c.1033T>A	XP_011524546.1:p.Phe345Ile
XM_011526244.2:c.1033T>A	XP_011524546.1:p.Phe345Ile
XM_011526245.1:c.910T>A	XP_011524547.1:p.Phe304Ile
XM_011526245.2:c.910T>A	XP_011524547.1:p.Phe304Ile
XM_017026064.1:c.910T>A	XP_016881553.1:p.Phe304Ile
XM_017026065.1:c.868T>A	XP_016881554.1:p.Phe290Ile
XM_017026066.1:c.808T>A	XP_016881555.1:p.Phe270Ile
XR_935263.1:n.1048T>A