Canonical Allele Identifier: CA2087395627

Gene: TNFSF11

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.42607866G= , CM000675.2:g.42607866G=	GRCh38
NC_000013.10:g.43182002G= , CM000675.1:g.43182002G=	GRCh37
NC_000013.9:g.42080002G=	NCBI36
NG_008990.1:g.50131G=

Transcript Alleles

HGVS	Amino-acid Change
NM_003701.4:c.*948G= MANE Select	NP_003692.1:n.*948G=
ENST00000398795.7:c.*948G= MANE Select	ENSP00000381775.3:n.*948G=
NM_003701.3:c.*948G=	NP_003692.1:n.*948G=
NM_033012.3:c.*948G=	NP_143026.1:n.*948G=
NM_033012.4:c.*948G=	NP_143026.1:n.*948G=
ENST00000398795.6:c.*948G=	ENSP00000381775.3:n.*948G=
ENST00000405262.6:c.*948G=	ENSP00000384042.2:n.*948G=
XM_011535280.1:c.*948G=	XP_011533582.1:n.*948G=
XM_011535280.2:c.*948G=	XP_011533582.1:n.*948G=
XM_017020802.1:c.*948G=	XP_016876291.1:n.*948G=
XM_017020803.2:c.*948G=	XP_016876292.1:n.*948G=