Canonical Allele Identifier: CA2308287716

Gene: TNFRSF11A

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.62365716G= , CM000680.2:g.62365716G=	GRCh38
NC_000018.9:g.60032949G= , CM000680.1:g.60032949G=	GRCh37
NC_000018.8:g.58183929G=	NCBI36
NG_008098.1:g.45402G= , LRG_194:g.45402G=

Transcript Alleles

HGVS	Amino-acid Change
NM_003839.4:c.731-992G= MANE Select	NP_003830.1:n.731-992G=
ENST00000586569.3:c.731-992G= MANE Select	ENSP00000465500.1:n.731-992G=
NM_001270949.1:c.731-992G=	NP_001257878.1:n.731-992G=
NM_001270949.2:c.731-992G=	NP_001257878.1:n.731-992G=
NM_001270950.1:c.730+3923G=	NP_001257879.1:n.730+3923G=
NM_001270950.2:c.730+3923G=	NP_001257879.1:n.730+3923G=
NM_001270951.1:c.616+5667G=	NP_001257880.1:n.616+5667G=
NM_001270951.2:c.616+5667G=	NP_001257880.1:n.616+5667G=
NM_001278268.1:c.689-992G=	NP_001265197.1:n.689-992G=
NM_001278268.2:c.689-992G=	NP_001265197.1:n.689-992G=
NM_003839.3:c.731-992G=	NP_003830.1:n.731-992G=
ENST00000269485.11:c.616+5667G=	ENSP00000269485.7:n.616+5667G=
ENST00000586569.2:c.731-992G=	ENSP00000465500.1:n.731-992G=
ENST00000616710.4:c.731-992G=	ENSP00000479567.1:n.731-992G=
ENST00000617039.4:c.730+3923G=	ENSP00000482466.1:n.730+3923G=
ENST00000639222.1:c.731-992G=	ENSP00000492422.1:n.731-992G=
XM_011526244.1:c.746-992G=	XP_011524546.1:n.746-992G=
XM_011526244.2:c.746-992G=	XP_011524546.1:n.746-992G=
XM_011526245.1:c.623-992G=	XP_011524547.1:n.623-992G=
XM_011526245.2:c.623-992G=	XP_011524547.1:n.623-992G=
XM_017026064.1:c.623-992G=	XP_016881553.1:n.623-992G=
XM_017026065.1:c.581-992G=	XP_016881554.1:n.581-992G=
XM_017026066.1:c.521-992G=	XP_016881555.1:n.521-992G=
XR_935263.1:n.761-992G=