Canonical Allele Identifier: CA8983880

Gene: TNFRSF11A

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.62368783C>T , CM000680.2:g.62368783C>T	GRCh38
NC_000018.9:g.60036016C>T , CM000680.1:g.60036016C>T	GRCh37
NC_000018.8:g.58186996C>T	NCBI36
NG_008098.1:g.48469C>T , LRG_194:g.48469C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_003839.4:c.866C>T MANE Select	NP_003830.1:p.Thr289Ile
ENST00000586569.3:c.866C>T MANE Select	ENSP00000465500.1:p.Thr289Ile
NM_001270949.1:c.783+2023C>T	NP_001257878.1:n.783+2023C>T
NM_001270949.2:c.783+2023C>T	NP_001257878.1:n.783+2023C>T
NM_001270950.1:c.730+6990C>T	NP_001257879.1:n.730+6990C>T
NM_001270950.2:c.730+6990C>T	NP_001257879.1:n.730+6990C>T
NM_001270951.1:c.616+8734C>T	NP_001257880.1:n.616+8734C>T
NM_001270951.2:c.616+8734C>T	NP_001257880.1:n.616+8734C>T
NM_001278268.1:c.824C>T	NP_001265197.1:p.Thr275Ile
NM_001278268.2:c.824C>T	NP_001265197.1:p.Thr275Ile
NM_003839.3:c.866C>T	NP_003830.1:p.Thr289Ile
ENST00000269485.11:c.616+8734C>T	ENSP00000269485.7:n.616+8734C>T
ENST00000586569.2:c.866C>T	ENSP00000465500.1:p.Thr289Ile
ENST00000616710.4:c.783+2023C>T	ENSP00000479567.1:n.783+2023C>T
ENST00000617039.4:c.730+6990C>T	ENSP00000482466.1:n.730+6990C>T
XM_011526244.1:c.881C>T	XP_011524546.1:p.Thr294Ile
XM_011526244.2:c.881C>T	XP_011524546.1:p.Thr294Ile
XM_011526245.1:c.758C>T	XP_011524547.1:p.Thr253Ile
XM_011526245.2:c.758C>T	XP_011524547.1:p.Thr253Ile
XM_017026064.1:c.758C>T	XP_016881553.1:p.Thr253Ile
XM_017026065.1:c.716C>T	XP_016881554.1:p.Thr239Ile
XM_017026066.1:c.656C>T	XP_016881555.1:p.Thr219Ile
XR_935263.1:n.896C>T