Canonical Allele Identifier: CA1630855945

Gene: TNFSF11

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.42581307G= , CM000675.2:g.42581307G=	GRCh38
NC_000013.10:g.43155443G= , CM000675.1:g.43155443G=	GRCh37
NC_000013.9:g.42053443G=	NCBI36
NG_008990.1:g.23572G=

Transcript Alleles

HGVS	Amino-acid Change
NM_003701.4:c.387+14G= MANE Select	NP_003692.1:n.387+14G=
ENST00000398795.7:c.387+14G= MANE Select	ENSP00000381775.3:n.387+14G=
NM_003701.3:c.387+14G=	NP_003692.1:n.387+14G=
NM_033012.3:c.168+14G=	NP_143026.1:n.168+14G=
NM_033012.4:c.168+14G=	NP_143026.1:n.168+14G=
ENST00000239849.8:c.246+14G=	ENSP00000239849.7:n.246+14G=
ENST00000358545.6:c.168+14G=	ENSP00000351347.2:n.168+14G=
ENST00000398795.6:c.387+14G=	ENSP00000381775.3:n.387+14G=
ENST00000405262.6:c.168+14G=	ENSP00000384042.2:n.168+14G=
ENST00000544862.5:c.168+14G=	ENSP00000444913.1:n.168+14G=
XM_011535280.1:c.168+14G=	XP_011533582.1:n.168+14G=
XM_011535280.2:c.168+14G=	XP_011533582.1:n.168+14G=
XM_017020802.1:c.225+14G=	XP_016876291.1:n.225+14G=
XM_017020803.2:c.168+14G=	XP_016876292.1:n.168+14G=