Canonical Allele Identifier: CA8983894

Gene: TNFRSF11A

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.62368871C>T , CM000680.2:g.62368871C>T	GRCh38
NC_000018.9:g.60036104C>T , CM000680.1:g.60036104C>T	GRCh37
NC_000018.8:g.58187084C>T	NCBI36
NG_008098.1:g.48557C>T , LRG_194:g.48557C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_003839.4:c.954C>T MANE Select	NP_003830.1:p.Tyr318=
ENST00000586569.3:c.954C>T MANE Select	ENSP00000465500.1:p.Tyr318=
NM_001270949.1:c.783+2111C>T	NP_001257878.1:n.783+2111C>T
NM_001270949.2:c.783+2111C>T	NP_001257878.1:n.783+2111C>T
NM_001270950.1:c.730+7078C>T	NP_001257879.1:n.730+7078C>T
NM_001270950.2:c.730+7078C>T	NP_001257879.1:n.730+7078C>T
NM_001270951.1:c.616+8822C>T	NP_001257880.1:n.616+8822C>T
NM_001270951.2:c.616+8822C>T	NP_001257880.1:n.616+8822C>T
NM_001278268.1:c.912C>T	NP_001265197.1:p.Tyr304=
NM_001278268.2:c.912C>T	NP_001265197.1:p.Tyr304=
NM_003839.3:c.954C>T	NP_003830.1:p.Tyr318=
ENST00000269485.11:c.616+8822C>T	ENSP00000269485.7:n.616+8822C>T
ENST00000586569.2:c.954C>T	ENSP00000465500.1:p.Tyr318=
ENST00000616710.4:c.783+2111C>T	ENSP00000479567.1:n.783+2111C>T
ENST00000617039.4:c.730+7078C>T	ENSP00000482466.1:n.730+7078C>T
XM_011526244.1:c.969C>T	XP_011524546.1:p.Tyr323=
XM_011526244.2:c.969C>T	XP_011524546.1:p.Tyr323=
XM_011526245.1:c.846C>T	XP_011524547.1:p.Tyr282=
XM_011526245.2:c.846C>T	XP_011524547.1:p.Tyr282=
XM_017026064.1:c.846C>T	XP_016881553.1:p.Tyr282=
XM_017026065.1:c.804C>T	XP_016881554.1:p.Tyr268=
XM_017026066.1:c.744C>T	XP_016881555.1:p.Tyr248=
XR_935263.1:n.984C>T